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HRID 1038660생성일: 2026년 10월 27일

Sulfuryl chloride → N-(2-chloro-3,5-dimethoxyphenyl)acetamide

https://huagongshe.com/reaction/1038660

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuryl chlorideHCID 24648—
반응물N-(3,5-dimethoxyphenyl)acetamideHCID 702039—
용매2-OxopropiononitrileHCID 69430—
생성물N-(2-chloro-3,5-dimethoxyphenyl)acetamideHCID 5659486851.5%

반응 단계

Sulfurylchloride (26.9 ml, 325 mmol, 1.93 eq.) is added (in 7 min) to a cold (0° C.) suspension of N-(3,5-dimethoxyphenyl)-acetamide (32.9 g, 169 mmol) in AcCN (500 ml), under an inert atmosphere. The resulting yellowish is allowed to stir 30 min and quenched by dropwise addition of a saturated aqueous solution of sodium bicarbonate (250 ml). The resulting precipitate is collected by vacuum filtration, washed with water (300 ml) and dried to afford 20 g of the desired product (batch 1). The filtrate is diluted with a saturated aqueous solution of sodium bicarbonate (300 ml) and extracted with EE (2×300 ml). The organic phase is washed with water and brine, dried (sodium sulphate), filtered and concentrated. The residue is purified by silica gel column chromatography (EE/Hx, 1:1→2:1) to provide 8.8 g of product (batch 2). Batch 1 and 2 are combined and stirred in hexane. The solid is collected by filtration, washed with hexane and dried to afford 25.8 g of the title compound as a white solid. ESI-MS: 264.0/266.0 [MH]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08552002B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-14a5db2084eb4075af69e4e58032d6e9
출처 메모uspto-grants-2013_10