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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1786281생성일: 2026년 10월 26일

Trichloroacetyl chloride → 3-(Benzyloxymethyl)-2,2-dichlorocyclobutanone

https://huagongshe.com/reaction/1786281

반응식

참여 물질

역할이름HCID투입량
반응물Trichloroacetyl chlorideHCID 6420—
반응물1,2-DimethoxyethaneHCID 8071—
반응물Allyl benzyl etherHCID 84542—
촉매ZincHCID 23994—
촉매Copper SulfateHCID 24462—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물3-(Benzyloxymethyl)-2,2-dichlorocyclobutanoneHCID 10355186—

반응 단계

Zinc dust (6.54 g, 0.1 mol) was suspended in water (30 ml) and argon bubbled through the suspension for 15 minutes before the addition of copper (II) sulphate (780 mg, 3.1 mmol). The reaction mixture was stirred at room temperature, under argon for 30 minutes. The mixture was filtered under a stream of argon and the solid washed with water (100 ml), acetone (100 ml) and dried in vacuo for 4 hours. The resultant zinc/copper couple was suspended in diethyl ether:1,2-dimethoxyethane (70 ml:10 ml) under argon and allyl benzyl ether (4.6 ml, 30 mmol) added. A solution of trichloroacetyl chloride (9 ml, 81 mmol) in diethyl ether:1,2-dimethoxyethane (58 ml:7 ml) was added dropwise over 45 minutes and the reaction mixture heated to reflux for 48 hours. The reaction mixture was filtered through Celite® and the salts washed with diethyl ether (3×70 ml). The filtrate was evaporated in vacuo and the residue redissolved in hexane (150 ml). The remaining solids were removed by filtration and the filtrate washed with a saturated aqueous solution of sodium hydrogen carbonate (2×100 ml), brine (80 ml), dried over magnesium sulphate, filtered and evaporated in vacuo. The crude material was purified by column chromatography over silica gel eluting with 10-25% hexane:diethyl ether. The title compound was obtained as a yellow oil (7.03 g, 27.3 mmol, 91%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07507742B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-d7985848d23b4f51ade2ab9ba36c2753
출처 메모uspto-grants-2009_03