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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233078생성일: 2026년 10월 26일

Benzyl Alcohol → 2-Furancarboxylic acid, tetrahydro-, phenylmethyl ester

https://huagongshe.com/reaction/233078

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물PyridineHCID 1049—
반응물Tetrahydro-2-furancarbonyl chlorideHCID 551254—
용매Diethyl EtherHCID 3283—
생성물2-Furancarboxylic acid, tetrahydro-, phenylmethyl esterHCID 11287208—

반응 단계

Tetrahydrofuroyl chloride (15.0 g, 112 mmol) was added dropwise to a cold solution of benzyl alcohol (10.9 g, 101 mmol) and pyridine (20.0 g, 253 mmol) in Et2O (200 mL). The solution was stirred at 0° for 40 minutes, then filtered to remove the side product pyridine hydrochloride. The filtrate was washed with 0.1M HCl (50 mL), saturated aqueous NaHCO3 (50 mL), and brine (50 mL), and then dried over MgSO4. Filtration and evaporation of the solvent gave a yellow oil, which was distilled. Benzyl tetrahydrofuroate was obtained as a colorless oil (21.1 g), b.p. 118° to 120° at 0.5 mm Hg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591846
출처 데이터셋uspto-grants-1997_01
ORD IDord-4d9fe164f77e42d2b03cb5c0f4ea08e2
출처 메모uspto-grants-1997_01