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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 584352생성일: 2026년 10월 25일

Triethylamine → m-Phenoxybenzyl cyanide

https://huagongshe.com/reaction/584352

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Phenoxybenzyl alcoholHCID 26295—
용매Ethyl AcetateHCID 8857—
용매Methanesulfonyl chlorideHCID 31297—
생성물m-Phenoxybenzyl cyanideHCID 4007532%

반응 단계

To a solution of 3-phenoxybenzylalcohol (25.0 g) and triethylamine (26.3 ml) in ethyl acetate (300 ml), methanesulfonyl chloride (14.6 ml) was added dropwise at 0° C. After stirring for 1 hour, the reaction mixture was washed with saturated aqueous sodium chloride, dried (MgSO4) and concentrated. The residue was dissolved in acetone (300 ml), admixed with sodium iodide (37.5 g) and then stirred for 1 hour. The reaction mixture was concentrated, and the residue was diluted with water and then extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4), and then concentrated. The residue was dissolved in dimethyl sulfoxide (100 ml) and stirred with sodium cyanide (7.35 g) for 15 hours at room temperature. The reaction mixture was diluted with ethyl acetate, washed with water, dried (MgSO4), and then concentrated. The residue was subjected to column chromatography on silica gel to obtain 3-phenoxyphenylacetonitrile (8.36 g, yield 32%) as an oil from a fraction eluted with ethyl acetate-hexane (1:7. v/v).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06924300B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-641bab9e2a0943d386ef1cd4bfeb9dbd
출처 메모uspto-grants-2005_08