戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 15729作成日:2026年10月25日

Ammonium Hydroxide → Benzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/15729

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物Ammonium ChlorideHCID 25517—
反応物Benzyl 3,4-dihydro-4-oxo-pyridine-1(2H)-carboxylateHCID 11368235—
反応物HCID 178478191HCID 178478191—
反応物HCID 178494437HCID 178494437—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Benzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylateHCID 59342393—

反応条件

温度-78 °C

反応手順

CuBr.SMe2 complex (1.49 g, 7.26 mmol) was added to 25 mL of anhydrous THF and cooled to −78° C. 4-Chlorophenylmagnesium bromide (7.26 mL, 1.0 M in THF, 7.26 mmol) was added slowly via syringe. Stirring at −78° C. for 1 hour produced an orange then green-like suspension. Boron trifluoride dimethyl etherate (0.92 mL, 7.26 mmol) was added and stirred for 5 minutes. To the newly formed complex was then added over 1 hour a solution of the compound 66 (1.0 g, 4.32 mmol) in 15 mL of anhydrous THF. After stirring 2 hours at −78° C., 16 mL of aq. 20% NH4Cl/conc. NH4OH (1:1) was added, and the mixture was allowed to warm-up to room temperature. EtOAc was used to extract (3×100 mL) and the combined organic layers were washed with brine and dried (MgSO4). Solvent was removed by rotary evaporation and the residue was purified by flash chromatography to give the product 67 as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732609B2
出典データセットuspto-grants-2010_06
ORD IDord-ab71bfae619241b3a6352d150f024773
出典メモuspto-grants-2010_06