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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477915생성일: 2026년 10월 25일

1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine → tert-butyl 8-(m-fluorophenyl)-4,5-dihydro-7-oxo-7H-thieno[2,3-a]quinolizine-10-carboxylate

https://huagongshe.com/reaction/477915

반응식

참여 물질

역할이름HCID투입량
반응물1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
반응물HCID 19020416HCID 19020416—
용매TolueneHCID 1140—
생성물tert-butyl 8-(m-fluorophenyl)-4,5-dihydro-7-oxo-7H-thieno[2,3-a]quinolizine-10-carboxylateHCID 19020443—

반응 단계

0.96 ml of N,N-dimethylformamide di-t-butyl acetal was added dropwise within 20 minutes to a boiling solution of 0.34 g of 4,5-dihydro-7-oxo-8-(m-fluorophenyl)-7H-thieno[2,3-a]quinolizine-10-carboxylic acid in 5 ml of toluene. The mixture was heated under reflux for an additional 30 minutes, left to stand at room temperature overnight and then washed once with water, twice with saturated aqueous sodium bicarbonate solution and once with saturated aqueous sodium chloride solution. The organic phase was dried over sodium sulfate and evaporated in vacuo. The residue was recrystallized from ethyl acetate and there was obtained tert-butyl 8-(m-fluorophenyl)-4,5-dihydro-7-oxo-7H-thieno[2,3-a]quinolizine-10-carboxylate of m.p. 135°-137°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04889848
출처 데이터셋uspto-grants-1989_12
ORD IDord-ac2f3f24dfe54c2b8418d4d430304963
출처 메모uspto-grants-1989_12