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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22288생성일: 2026년 10월 23일

Acetic Anhydride → HCID 54082237, 화합물

https://huagongshe.com/ko/reaction/22288

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물1-Benzylpiperidine-4-carbaldehydeHCID 89584—
반응물Lithium diisopropylamideHCID 2724682—
반응물3,4-Dihydrocyclopenta(b)indol-1(2H)-oneHCID 6424669—
용매TetrahydrofuranHCID 8028—
생성물HCID 54082237HCID 54082237—

반응 조건

온도-78 °C

반응 단계

To a mixture of 1,2,3,4-tetrahydrocyclopent[b]-indol-1-one (440 mg, 2.6 mmol) and 1-benzylpiperidine-4-carboxaldehyde (581 mg, 2.86 mmol) in 90 ml dry THF was added 5.4 mmol of lithium diisopropylamide at -78° C. The mixture was stirred at -78° C. for 30 minutes, then warmed up to 0° C. for 1.5 hours, and then to r.t. for 15 minutes. Acetic anhydride (0.265 g, 2.6 mmol) was added, the mixture was stirred at r.t. for 1.5 hours and quenched ammonium chloride, water and extracted with chloroform. The organic layer was dried, concentrated, and purified through silica gel to give the title compound. 1HNMR (CDCl3)δ 1.45-1.7 (m, 3H), 1.8-2.3 (m, 4H), 2.8-3.0 (m, 2H), 3.46 (s, 2H), 3.55 (s, 2H), 6.5 (m, 1H), 7.1-7.4 (m, 8H), 7.9 (m, 1H), 9.2 (s, 1H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428043
출처 데이터셋uspto-grants-1995_06
ORD IDord-38dbbafc6f744e7f8c4c06aaaa9e7d7c
출처 메모uspto-grants-1995_06