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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 398419생성일: 2026년 10월 24일

Ethyl (4-chlorophenyl)acetate → HCID 46221154, 화합물

https://huagongshe.com/ko/reaction/398419

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl (4-chlorophenyl)acetateHCID 84177—
반응물Lithium diisopropylamideHCID 2724682—
반응물(Iodomethyl)cyclopentaneHCID 2762531—
용매HexamethylphosphoramideHCID 12679—
용매tetrahydrofuran HMPAHCID 86583969—
생성물HCID 46221154HCID 4622115490.9%

반응 조건

온도-78 °C

반응 단계

A solution of freshly prepared lithium diisopropylamide (23.0 mL of 0.31M stock solution, 7.13 mmol) cooled to −78° C. was treated with (4-chloro-phenyl)-acetic acid ethyl ester (1.28 g, 6.48 mmol) in tetrahydrofuran/hexamethylphosphoramide (16.1 mL, 3:1). The resulting solution was stirred at −78° C. for 45 min. At this time, the reaction was treated with a solution of iodomethylcyclopentane (1.50 mg, 7.13 mmol) in hexamethylphosphoramide (1 mL). The reaction-mixture was stirred at −78° C. for 4 h. The reaction was warmed to 25° C. and stirred at 25° C. for 16 h. The reaction mixture was then quenched by the dropwise addition of a saturated aqueous ammonium chloride solution (20 mL). This mixture was poured into water (100 mL) and extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 75/25 hexanes/ethyl acetate) afforded 2-(4-chloro-phenyl)-3-cyclopentyl-propionic acid ethyl ester (1.65 g, 90.9%) as a yellow oil: EI-HRMS m/e calcd for C16H21Cl2O2 (M+) 280.1230, found 280.1227.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610846B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-6c8c483c00954e319776c71002fb2ab0
출처 메모uspto-grants-2003_08