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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1938111생성일: 2026년 10월 26일

Lauric Acid → (+)-2-{4-(1-Dodecanoyloxyethyl)phenyl}-5-decyloxypyrimidine

https://huagongshe.com/reaction/1938111

반응식

참여 물질

역할이름HCID투입량
반응물Lauric AcidHCID 3893—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물4-PyrrolidinopyridineHCID 75567—
반응물2-(4-(1-Hydroxyethyl)phenyl)-5-decyloxypyrimidineHCID 21468280—
용매DichloromethaneHCID 6344—
생성물(+)-2-{4-(1-Dodecanoyloxyethyl)phenyl}-5-decyloxypyrimidineHCID 2146829594%

반응 단계

Into 20 ml of dichloromethane were dissolved 1.78 g (5 millimoles) of the (+)-2-{4-(1-hydroxyethyl)phenyl}-5-decyloxypyrimidine obtained in Preparation Example [starting material compound (VI)] 70 and 1.2 g (6 millimoles) of dodecanic acid, and then 1.4 g of N,N'-dicyclohexylcarbodiimide and 0.1 g of 4-pyrrolidinopyridine were added thereto, followed by stirring at room temperature for 24 hours. After completion of the reaction, the precipitates were filtered off and 200 ml of toluene were added thereto, followed by washing with water, 5% acetic acid, water, 5% aqueous sodium hydrogen carbonate solution and water in this order. After the organic phase was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent; toluene:ethyl acetate) to obtain 2.53 g (yield: 94%) of (+)-2-{4-(1-dodecanoyloxyethyl)phenyl}-5-decyloxypyrimidine. The physical values are shown in Table-1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05693251
출처 데이터셋uspto-grants-1997_12
ORD IDord-a5a409c04ed542e3a58f8a2daf4c7b5e
출처 메모uspto-grants-1997_12