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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1764721생성일: 2026년 10월 25일

Methanol → 3-nitro-5-oxo-6,7,8,9-tetrahydro [5H] benzocycloheptene-7-carbonitrile

https://huagongshe.com/reaction/1764721

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Acetone CyanohydrinHCID 6406—
반응물Potassium CarbonateHCID 11430—
반응물8,9-dihydro-3-nitro-5H-benzocyclohepten-5-oneHCID 20094732—
용매TetrahydrofuranHCID 8028—
생성물3-nitro-5-oxo-6,7,8,9-tetrahydro [5H] benzocycloheptene-7-carbonitrileHCID 54523296—

반응 조건

온도90 °C

반응 단계

A mixture of 50 g of 3-nitro-8,9-dihydro [5H] benzocycloheptene-5-one, 1200 ml of methanol, 120 ml of tetrahydrofuran, 100 ml of a 10% aqueous potassium carbonate and 50 ml of acetone cyanhydrin under nitrogen was refluxed for an hour in a bath at 90° C. and the mixture was concentrated to about 200 ml under reduced pressure. The mixture was cooled to 20° C. and was extracted with methylene chloride. The organic phase was washed with water, dried and distilled to dryness under reduced pressure. The 58 g of brown oil residue were crystallized from 50 ml of methanol and the mixture was vacuum filtered to obtain 46 g of 3-nitro-5-oxo-6,7,8,9-tetrahydro [5H] benzocycloheptene-7-carbonitrile with a melting point of 107° C. and then 120° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04117164
출처 데이터셋uspto-grants-1978_09
ORD IDord-2b0346b56d1d41af8c8e1dd4e1b2dc2c
출처 메모uspto-grants-1978_09