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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7073생성일: 2026년 10월 24일

Acetyl chloride → 4-acetoxy-N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-3-methoxyphenylacetamide

https://huagongshe.com/ko/reaction/7073

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물TriethylamineHCID 8471—
반응물N-[3-(4-tert-Butylcyclohexan-1-yl)phenyl]-4-hydroxy-3-methoxyphenylacetamideHCID 22019581—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물4-acetoxy-N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-3-methoxyphenylacetamideHCID 2201960881.4%

반응 조건

온도25 °C

반응 단계

N-[3-(4-tert-Butylcyclohexan-1-yl)phenyl]-4-hydroxy-3-methoxyphenylacetamide (100 mg) obtained in Example 20, triethylamine (94 mg) and 4-dimethylaminopyridine (5 mg) are dissolved in methylene chloride (5 ml), and thereto is added dropwise acetyl chloride (40 mg) under ice-cooling. The mixture is stirred at 25° C. for 18 hours, and the reaction solution is washed with water. The organic layer is dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give the desired compound (90 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084176B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-475396a544d2493ca1fa498aca729fbe
출처 메모uspto-grants-2006_08