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HRID 16602作成日:2026年10月27日

Benzyl Alcohol → tert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamate

https://huagongshe.com/reaction/16602

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物Sodium IodideHCID 5238—
反応物3-Chloro-2,2-dimethylpropanoyl chlorideHCID 61345—
反応物DiisopropylethylamineHCID 81531—
反応物Tert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
反応物Benzyl 3-chloropivalateHCID 54294282—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamateHCID 866021211.3%

反応条件

温度120 °C

反応手順

To a stirred solution of tert-butyl (piperidin-4-ylmethyl)carbamate (38.8 g, 181 mmol) in N,N-dimethylformamide (100 mL) was added benzyl 3-chloropivalate {14.2 g, 124 mmol, prepared from 3-chloropivaloyl chloride (25.6 g, 165 mmol) and benzyl alcohol (19.6 g, 181 mmol), ethyldiisopropylamine (64.0 g, 495 mmol) and sodium iodide (27.1 g, 181 mmol) at ambient temperature. The resulting mixture was stirred at 120° C. for 14 h. The volatile components were removed by evaporation and the resulting residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (1:1) to give 640 mg (1%) of the title compound as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737163B2
出典データセットuspto-grants-2010_06
ORD IDord-51017605c27a4df0905c4c42548db89d
出典メモuspto-grants-2010_06