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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 414825생성일: 2026년 10월 26일

Water → HCID 14349113, 화합물

https://huagongshe.com/reaction/414825

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물1,2-Dichloro-4-fluorobenzeneHCID 74028—
반응물HCID 13118512HCID 13118512—
생성물HCID 14349113HCID 1434911357%

반응 조건

온도60 °C

반응 단계

A solution of 7,8-dimethoxy-1-hydroxy-2,3,4,5-tetrahydro-3-benzazepine (3 g, 13.4 mmole) in 25 ml dimethylformamide was slowly dropped into a stirring suspension of sodium hydride (50% oil dispersion, 0.7 g, 14.8 mmole), previously washed with hexane, in 10 ml dimethylformamide. After the addition was completed, the mixture was warmed for one hour at 60° C., then was cooled and a solution of 3,4-dichlorofluorobenzene (2.4 g, 14.8 mmole) in 10 ml dimethylformamide was added. After stirring two hours at ambient temperature, the reaction mixture was stirred with 400 ml water and was extracted with ethyl acetate. The organic extract was washed with ethyl acetate. The organic extract was washed with water and saturated NaCl and was dried (anhydrous MgSO4), filtered and evaporated to 7 g of an oil. This oil was purified by HPLC (silica gel, 5% methanol in dichloromethane) to give 2.8 g (57%) of an oil. This oil was converted to the oxalate salt as in Example 1 and was recrystallized from ethyl acetate-methanol to give 2.1 g (34%) of 1,(3-4-dichlorophenoxy)-7,8-dimethoxy-2,3,4,5-tetrahydro-3-benzazepine oxalate, d 167°-168° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04794181
출처 데이터셋uspto-grants-1988_12
ORD IDord-ec49c880435b4f18b7729301aa2b6e48
출처 메모uspto-grants-1988_12