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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356174생성일: 2026년 10월 24일

Chloroacetyl chloride → (3aR*,10aS*)-9-Benzyl-4-(chloroacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one

https://huagongshe.com/ko/reaction/356174

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참여 물질

역할이름HCID투입량
반응물Chloroacetyl chlorideHCID 6577—
반응물(3aR*,10aS*)-9-benzyl-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta [e][1,4]diazepin-10(1H)-oneHCID 70109795—
용매1,2-DichloroethaneHCID 11—
생성물(3aR*,10aS*)-9-Benzyl-4-(chloroacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-oneHCID 7011019288%

반응 단계

On a water-bath kept at 14° C., to a solution of (3aR*,10aS*)-9-benzyl-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one (5.85 g, 20 mmol) in 1,2-dichloroethane (20 mL) was added dropwise a solution of chloroacetyl chloride (2.5 g, 22 mmol) in 1,2-dichloroethane (15 mL), and the mixture was stirred for 10 minutes. The aqueous layer of this mixture was separated, and the organic layer was washed with water and a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, which was subjected to filtration, and the filtrate was concentrated under reduced pressure. The concentrate was recrystallized from dichloromethane-hexane to give 6.49 g (yield 88%) of the titled compound, m.p. 154°-156° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05834463
출처 데이터셋uspto-grants-1998_11
ORD IDord-ff6fcf84233f492ebcd5935e0b4a2bcf
출처 메모uspto-grants-1998_11