• 공업화학
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• 제5권1호
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• pp.114-120
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• 1994

DCI (dichlorolsocyanuric acid sodium salt)에 의한 PNPDPP (p-nitrophenyldiphenylphosphate)의 미셀 내에서의 분해 반응을 pH 8.0 borate 완충용액에서 속도론적으로 살펴보았다. 양이온성 계면활성제인 CTAC (cetyltrimethylammonium chloride) 또는 CTAB (cetyltrimethylammonium bromide)를 첨가하면 반응은 빠르게 촉진되었으며, 특히 CTAB의 경우는 DCI의 N-Cl 결합이 N-Br 결합으로 전환되어 반응이 진행되었다.

• 약학회지
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• 제36권2호
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• pp.126-128
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• 1992

A new method for felbinac, which is a potent anti-inflammatory agent, is described. Friedel-Crafts reaction of biphenyl with ethyl ${\alpha}-chloro-{\alpha}-(methylthio)acetate(1)$ afforded ethyl 2-methylthio-2-(4-biphenylyl)acetate(4). Felbinac (7) was synthesized by desulfurization of compound (4) with zinc dust in acetic acid, followed by hydrolysis of the resultant ethyl 2-(4-biphenylyl)acetate (6).

• KSBB Journal
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• 제5권4호
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• pp.397-402
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• 1990

Hydrolysis of inulin was investigated employing various commercially available resin catalysts for the production of high grade fructose syrup. The particle size and porosity of the resin significantly affected the distribution of the products, indicating that the intraparticle diffusion of reactants controls thc selectivity as well as the reaction rate. To confirm the effect of the intraparticle diffusion, two different types of resin catalysts were prepared: the one having sulfonic acid group distributed uniformly throughout genular microparticles (A-type) and the other having sulfonic acid group located mainly at the exterior surface of genular microparticles (E-type). The results were found that the reaction rate and the selectivity of the E-type catalyst were higher than those of the A-type catalyst.

• 약학회지
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• 제33권4호
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• pp.237-240
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• 1989

A new synthetic method for tiaprofenic acid, which is a potent anti-inflammatory agent, was described. Friedel-Crafts reaction of thiophene with ethyl ${\alpha}-chloro-{\alpha}-(methylthio)$ acetate (1) gave ethyl ${\alpha}-methylthio-2-thiopheneacetate$ (3). Ethyl ${\alpha}-methyl-2-thiopheneacetate$ (5) was prepared by treatment of (3) with NaH and MeI, followed by desulfurization with zinc dust-acetic acid of the resultant ethyl ${\alpha}-methyl-{\alpha}-methylthio-2-thiopheneacetate$ (4). Tiaprofenic acid (7) could be easily synthesized by benzoylation of (5) and hydrolysis of the resultant ethyl $5-benzoyl-{\alpha}-methyl-2-thiopheneacetate$ (6).

• 약학회지
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• 제36권2호
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• pp.137-139
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• 1992

A new method for xenbucin, which is a antihypercholesteremic agent, is described. Friedel-Crafts reaction of biphenyl with ethyl ${\alpha}-chloro-{\alpha}-(methylthio)acetate(1)$ afforded ethyl 2-methylthio-2-(4-biphenylyl)acetate(2). Ethyl 2-(4-biphenylyl)butyrate(4) was obtained by ethylation of (2) with NaH and $C_2H_5I$, followed by desulfurization of the resultant ethyl 2-methylthio-2-(4-biphenylyl)butyrate(3) with zinc dust in acetic acid. Xenbucin was synthesized by hydrolysis of (4).

• 한국세라믹학회지
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• 제28권8호
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• pp.611-618
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• 1991

In the present study adding hydroxypropyl celluose as dispersant to the ethanol solution of Zr-butoxide prior to starting the hydrolysis reaction, spherical and submicrometer sized hydrated zirconia powders were synthesized successfully. But syntesized hydrated zirconia powders were soluble considerably in ethanol used as washing medium. Washing once the powder with plenty amount of water after washing thrice it with acetone, reaction mother solution remained between the particles was effectively removed and the particles were converted to insoluble state to ethanol at the same time. As a result of such washing processes it was able to prevent the formation of polydispersed, agglomerated and multiplet particles almost always even when such concentrated solutions of Zr-n-butoxide as 0.5 M were hydrolyzed.

• Bulletin of the Korean Chemical Society
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• 제22권7호
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• pp.689-692
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• 2001

An imprinting technique with labile covalent interactions has been developed in the design of new polymer catalysts. The template monomer 2 was prepared and copolymerized with DVB or EDMA to provide the polymer with a cavity having the shape of th e transition state of the reaction as well as binding sites for the substrate and catalytic functionalities. The rate of hydrolysis of diphenyl carbonate (1) in the presence of the imprinted polymer IP-DVB-THF was found to be 120 times faster than the background uncatalyzed reaction. A Km of 32 mM and a kcat of 1.8 ${\times}$ 10-3min-1 were observed from Michaelis-Menten kinetics with the imprinted polymer IP-DVB-THF.

• 한국환경과학회지
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• 제17권5호
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• pp.509-516
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• 2008

New functional surfactant, N,N-dimethyl-N-dodecyl-N-(2-methyl benzimidazoyl) ammonium chloride(DDBAC) having benzimidazole(BI) functional group have been synthesized and the critical micellar concentration of DDBAC measured by surface tentiometry and electric conductivity method was $8.9{\times}10^{-4}M$. Micellar effects in DDBAC functional surfactant solution on the hydrolysis of p-nitrophenylacetate(p-NPA), p-nitro-phenylpropionate(p-NPP) and p-nitrophenylvalerate(p-NPV) were observed with change of various pH (Tris-buffer). The pseudo first rate constants of hydrolysis of p-NPA, p-NPP and p-NPV in optimum concentration of DDBAC solution increase to about 160, 280 and 600 times, respectively, as compared with those of aqueous solution at pH 8.00(Tris-buffer). It is considered that benzimidazole functional moiety accelerates the reaction rates of hydrolysis because they act as nucleophile or general base. In optimum concentration of DDBAC solution, the rate constants of hydrolysis of p-NPP and p-NPV increase to about 1.5 and 3.0 times, respectively, as compared with that of p-NPA. It means that the more the carbon numbers of alkyl group of substrates, the larger the binding constants between DDBAC micelle and substrates are. To know the hydrolysis mechanism of p-NPCE(p-NPA, p-NPP and p-NPV), the deuterium kinetic isotope effects were measured in $D_2O$ solutions. Consequently the pseudo first order rate constant ratios in $H_2O$ and $D_2O$ solution, $k_{H_2O}/k_{D_2O}$, were about $2.8{\sim}3.0$ range. It means that the mechanism of hydrolysis were proceeded by nucleophile and general base attack in approximately same value.

• 한국식품영양과학회지
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• 제21권5호
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• pp.513-518
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• 1992

탈지유채박(Brassica napus var. Youngsan)으로부터 추출, 정제하여 얻어진 유채단백질을 효소로 가수분해하기 위한 최적조건에 대하여 검토하였다. Pronase가 유채단백질에서 alcalase, neutrase보다 높은 활성을 나타내었고, 유채단백질의 가열처리는 pronase의 활성을 감소시켰다. 또한 유채단백질의 가수분해도는 완충액보다는 증류수에서 더 높은 결과를 얻었다. 시간별로는 1시간까지는 급속히 반응이 일어나나 그 이후는 완만해졌다. Pronase에 의한 유채단백질의 가수분해 최적조건은 $40^{\circ}C$와 pH 8.0이었고 효소 대 기질의 비와 기질 농도는 각각 1/100(w/w), 1%(w/v)이었다. 이와 같은 조건하에서 Km은 3.48%(w/v)를 얻었다.

• 한국미생물·생명공학회지
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• 제26권3호
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• pp.264-268
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• 1998

덱스트란수크라제는 Sucrose를 이용하여 덱스트란의 합성을 촉진하는데 sucrose이외에 다른 탄수화물이 효소 반응기 중에 존재하는 경우에는 Sucrose의 glucose를 이 탄수화물에 전달하는 반응을 촉진하여 새로운 구조의 산물을 생산한다. Leuconostoc mesenteroides B-742CB로 부터 얻은 덱스트란수크라제를 이용하여 플루란을 변형하고 그 조건을 최적화 하고자 했다. 수용성 변형 플루란은 이론적 수율의 57%(<$\pm$5)를 얻었다. 플루란 변형의 최적 조건으로는 pH 5.2, 28$^{\circ}C$ 에서 기질 0.37%(w/v)와 반응한 효소의 농도와 Sucrose농도가 각각 0.1 U/$m\ell$과 48mM일 때였다. 변형 플루란을 pullulanase, endodextranase로 처리하여 변형 전의 플루란과가수분해 상태를 비교 분석한 결과 변형전의 산물에 비해 이들 가수 분해 효소에 대해 더 저항성을 보였다. 변형 플루란을 methylation과 산가수분해 후 TLC한 결과 sucrose의 glucose가 플루란 glucose의 C3, C4, C6 위치의 free-OH group에 수식된 새로운 구조의 변형 플루란임을 확인하였다.