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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 729360생성일: 2026년 10월 25일

Benzyl Alcohol → Pentafluorobenzoic acid, benzyl ester

https://huagongshe.com/reaction/729360

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물Pentafluorobenzoic acidHCID 11770—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
용매Sodium chloride; waterHCID 57417360—
생성물Pentafluorobenzoic acid, benzyl esterHCID 51785677.3%

반응 조건

온도0 °C

반응 단계

A solution of 2,3,4,5,6-pentafluorobenzoic acid (15.25 g, 71.9 mmol), 4-dimethylaminopyridine (4.4 g, 36.0 mmol) and benzyl alcohol (7.4 mL, 71.5 mmol) in dichloromethane (150 mL) is cooled to 0° C. under an inert atmosphere. 1-[3-(Dimethylamino)propyl]-3-ethyl carbodiimide hydrochloride (16.7 g, 87.1 mmol) is added and the mixture stirred at 0° C. for 2 hours. The mixture is warmed to ambient temperature, stirred for 24 hours, and then poured into brine. The mixture is extracted with chloroform and the organic phase washed with NaHCO3, dried over Na2SO4, filtered and concentrated under vacuum to yield the title compound as a white solid (16.7 g). This material is used without further purification. 1H NMR (CDCl3): δ 7.49-7.27 (m, 5H), 5.40 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582627B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-bf56666aa0ca4581ad3c2f56c7c7d28f
출처 메모uspto-grants-2009_09