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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1770062생성일: 2026년 10월 26일

Dicyclohexylcarbodiimide → (+)-4-[3-{2(S)-methylbutoxy}propyl]phenyl 4-decyloxybenzoate

https://huagongshe.com/reaction/1770062

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물4-PyrrolidinopyridineHCID 75567—
반응물4-(Decyloxy)benzoic acidHCID 138527—
반응물(+)-4-[3-{2(S)-methylbutoxy}propyl]phenolHCID 22844682—
생성물(+)-4-[3-{2(S)-methylbutoxy}propyl]phenyl 4-decyloxybenzoateHCID 2284468390.4%

반응 단계

Into a four-necked flask equipped with a stirrer and a thermometer were charged 1.11 g (5 millimole) of (+)-4-[3-{2(S)-methylbutoxy}propyl]phenol, 1.67 g (6 millimole) of 4-decyloxybenzoic acid and 30 ml of anhydrous dichlomethane, and then 1.22 g (6 millimole) of N,N'-dicyclohexylcarbodiimide and 0.1 g of 4-pyrrolidinopyridine were added thereto, followed by stirring at room temperature for one day. After completion of the reaction, precipitates formed were filtered off and diluted with 200 ml of toluene. The organic phase was washed with water, 5% aqueous acetic acid solution, water, 5% aqueus sodium hydrogen carbonate solution and water in this order and then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromttography (eluent: toluene-ethyl acetate) to obtain 2.18 g (yield: 90.4%) of (+)-4-[3-{2(S)-methylbutoxy}propyl]phenyl 4-decyloxybenzoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05385693
출처 데이터셋uspto-grants-1995_01
ORD IDord-b3b5a101e514463a82fb6d1fda8d861a
출처 메모uspto-grants-1995_01