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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1759419생성일: 2026년 10월 26일

4-Toluenesulfonyl chloride → O-(p-toluenesulfonyl)-m-phenoxymandelonitrile

https://huagongshe.com/reaction/1759419

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물Sodium CyanideHCID 8929—
반응물3-PhenoxybenzaldehydeHCID 38284—
용매EthanolHCID 702—
생성물O-(p-toluenesulfonyl)-m-phenoxymandelonitrileHCID 1294513650.3%

반응 단계

A mixture of 3.96 g of m-phenoxybenzaldehyde and 3.97 g of p-toluenesulfonyl chloride was stirred under ice cooling, and 10 ml of an aqueous solution containing 1.47 g of sodium cyanide was added dropwise over 30 minutes. Then, 10 ml of ethanol was added, and the mixture was stirred for 30 minutes under ice cooling, and then at room temperature for 30 minutes. The mixture was extracted with 30 ml of methylene chloride three times. The extract was washed with 20 ml of water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Recrystallization of the residue from ethanol afforded 3.816 g of O-(p-toluenesulfonyl)-m-phenoxymandelonitrile. The mother liquor was concentrated under reduced pressure, and the residue was purified by column chromatography (silica gel; hexane and benzene) to afford 1.846 g of O-(p-toluenesulfonyl)-m-phenoxymandelonitrile. The total amount of the product was 5.662 g (yield 75%). The product was in the form of colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04340740
출처 데이터셋uspto-grants-1982_07
ORD IDord-6f0ed9bd60d04364974838efcbae9a41
출처 메모uspto-grants-1982_07