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HRID 380128作成日:2026年10月26日

2-Bromo-1,2-diphenylethan-1-one → 2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate

https://huagongshe.com/reaction/380128

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-1,2-diphenylethan-1-oneHCID 102630—
反応物SodiumHCID 5360545—
反応物1-(3-Benzyloxybenzoyl)-2-piperidinecarboxylic acidHCID 18367416—
触媒Sulfuric AcidHCID 1118—
溶媒EthanolHCID 702—
生成物2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylateHCID 5424785628.4%

反応条件

温度70 °C

反応手順

Sodium (54 mg) was dissolved in ethanol (8.0 ml), and then 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylic acid (665 mg), conc. sulfuric acid (1 drop), and desyl bromide (539 mg) was successively dissolved thereto. The resulting mixture was stirred at 70° C. for 2 days, cooled to room temperature, and partitioned between ethyl acetate and 1N HCl. The organic layer was washed with 1N HCl, aqueous sodium bicarbonate, and brine, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed over silica gel to afford 2-oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate (297 mg) as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06300344B1
出典データセットuspto-grants-2001_10
ORD IDord-969536c747cd4b3a94fb701bec284060
出典メモuspto-grants-2001_10