돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 726696생성일: 2026년 10월 25일

Dimethyl Sulfate → 5-methoxy-1-tosyl-2,3-dihydro-1H-1-benzazepine

https://huagongshe.com/reaction/726696

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfateHCID 6497—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물1-Tosyl-3,4-dihydro-1H-benzo[b]azepin-5(2H)-oneHCID 266852—
용매DimethylformamideHCID 6228—
생성물5-methoxy-1-tosyl-2,3-dihydro-1H-1-benzazepineHCID 11381909—

반응 단계

In 10 ml of dimethylformamide was suspended 165 mg of 60% sodium hydride, and 1.0 g of 1-tosyl-2,3,4,5-tetrahydro-1-H-1 -benzazepin-5-one was added to the suspension under ice-cooling, followed by 1 hour of stirring in the ice bath. To this was added dropwise 0.90 ml of dimethyl sulfate, and the mixture was stirred for 30 minutes. After adding ammonium chloride aqueous solution to the reaction solution and subsequently evaporating the solvent, the thus obtained residue was treated with chloroform and water to effect phase separation, and the resulting organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated and the resulting residue was applied to column chromatography, which was eluted with hexane-ethyl acetate (4:1, v/v) to obtain 621 mg of 5-methoxy-1-tosyl-2,3-dihydro-1H-1-benzazepine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05710150
출처 데이터셋uspto-grants-1998_01
ORD IDord-19a228057e4c429da16d281f45916afa
출처 메모uspto-grants-1998_01