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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 465612생성일: 2026년 10월 25일

Bromoacetonitrile → 7-Cyano-5-oxoheptanoic acid

https://huagongshe.com/reaction/465612

반응식

참여 물질

역할이름HCID투입량
반응물BromoacetonitrileHCID 11534—
반응물4-Acetylbutyric acidHCID 18407—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
용매TetrahydrofuranHCID 8028—
생성물7-Cyano-5-oxoheptanoic acidHCID 14986712—

반응 단계

To a solution of potassium hexamethyldisilazide (66 ml, 60 mmol) in dry tetrahydrofuran (140 ml) at -70° is added slowly 5-oxohexanoic acid (36 ml, 30 mmol). The resulting yellow suspension is stirred at -70° for 1 h and bromoacetonitrile (2.2 ml, 32 mmol) is added slowly. The reaction mixture is stirred at -70° for 1 h and then at room temperature for 0.5 h. The reaction is quenched by addition of 1N aqueous hydrochloric acid (100 ml). The aqueous layer is extracted twice with ether. Combined organic layer is dried, filtered and evaporated to obtain a dark oil which is purified by silica gel chromatography using 9:1 ether/hexane with 1% acetic acid as eluent to give 7-cyano-5-oxoheptanoic acid as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05153214
출처 데이터셋uspto-grants-1992_10
ORD IDord-8b89643d0bdd44568e4cd81cca446028
출처 메모uspto-grants-1992_10