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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1009095생성일: 2026년 10월 25일

Tetrakis(hydroxymethyl)phosphonium chloride → 2,2-Dimethoxyethylcyclopent-3-enol

https://huagongshe.com/reaction/1009095

반응식

참여 물질

역할이름HCID투입량
반응물Tetrakis(hydroxymethyl)phosphonium chlorideHCID 31298—
반응물4-(2,2-Dimethoxyethyl)hepta-1,6-dien-4-olHCID 86614113—
촉매HCID 178425456HCID 178425456—
용매WaterHCID 962—
용매IsopropanolHCID 3776—
용매DichloromethaneHCID 6344—
용매Sodium HydroxideHCID 14798—
생성물2,2-Dimethoxyethylcyclopent-3-enolHCID 67306500—

반응 단계

A solution of 4-(2,2-dimethoxyethyl)hepta-1,6-dien-4-ol (28 g, 140 mmol) in DCM (2 L) was charged to a 3 L RB flask. Dry argon was bubbled through the solution for ˜30 minutes. Grubbs second generation catalyst (5.9 g, 7.0 mmol) was added and the reaction was allowed to stir under argon for 15 hours. The reaction was quenched with a solution of tetrakis-(hydroxymethyl)phosphonium chloride (27 g, 140 mmol) in isopropanol (200 mL) and 10 N NaOH (14 mL), and stirred for 15 hours. The reaction was diluted with water (1 L) and poured into a seperatory funnel. The DCM layer was separated and the aqueous was extracted with DCM (3×100 mL). The combined organics were concentrated to a dark oil which was purified by flash chromatography on a 330 g ISCO column eluting by gradient hexanes to 20% EtOAc/hexanes over a 50 minute period. Product fractions were combined to afford the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07973047B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-2d83a5ed07d74287b7298e1263f209aa
출처 메모uspto-grants-2011_07