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HRID 602129作成日:2026年10月24日

Potassium Bromide → Benzyl 3-formylpiperidine-1-carboxylate

https://huagongshe.com/ja/reaction/602129

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium BromideHCID 253877—
反応物Sodium BicarbonateHCID 516892—
反応物Benzyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2776577—
反応物Sodium HypochloriteHCID 23665760—
触媒TempoHCID 2724126—
溶媒DichloromethaneHCID 6344—
生成物Benzyl 3-formylpiperidine-1-carboxylateHCID 989965390%

反応手順

An aqueous solution (2 mL) of potassium bromide (983 mg, 8.26 mmol) was added to 1-benzyloxycarbonyl-3-piperidinyl methanol (2.00 g, 8.02 mmol) and 2,2,6,6-tetramethyl piperidine-N-oxyl (12.5 mg, 0.0802 mmol) in dichloromethane (20 mL). The mixture was stirred for 5 min while chilled in an ice bath. A 0.35 mol/L aqueous sodium hypochlorite solution (25.2 mL, 8.82 mmol) and sodium bicarbonate (1.96 g, 23.3 mmol) were added and the mixture was stirred for 10 min. Subsequently, the reaction mixture was extracted with ethyl acetate and the extract washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the residue by silica gel column chromatography (hexane:ethyl acetate=10:1->2:1) gave 1.78 g (90%) of the desired compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902367B2
出典データセットuspto-grants-2011_03
ORD IDord-6e270006b9de40f4a66816fc7ecc256c
出典メモuspto-grants-2011_03