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HRID 22288作成日:2026年10月25日

Acetic Anhydride → HCID 54082237、化合物

https://huagongshe.com/reaction/22288

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物1-Benzylpiperidine-4-carbaldehydeHCID 89584—
反応物Lithium diisopropylamideHCID 2724682—
反応物3,4-Dihydrocyclopenta(b)indol-1(2H)-oneHCID 6424669—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 54082237HCID 54082237—

反応条件

温度-78 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428043
出典データセットuspto-grants-1995_06
ORD IDord-38dbbafc6f744e7f8c4c06aaaa9e7d7c
出典メモuspto-grants-1995_06