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HRID 29758作成日:2026年10月24日

Triethylamine → Tert-butyl trans-4-(N-methoxy-N-methylcarbamoyl)cyclohexylcarbamate

https://huagongshe.com/ja/reaction/29758

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物N,O-DimethylhydroxylamineHCID 14232—
反応物4-(((Tert-butoxy)carbonyl)amino)cyclohexane-1-carboxylic acidHCID 2755996—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl trans-4-(N-methoxy-N-methylcarbamoyl)cyclohexylcarbamateHCID 2472092861%

反応手順

A solution of 4-[N-(tert-butoxycarbonyl)amino]-cyclohexane carboxylic acid (11.95 g, 49.0 mmol), O,N-dimethylhydroxylamine (4.88 g, 50.0 mmol), DCC (9.60 g, 50 mmol) and triethylamine (5.06 g, 50.0 mmol) in DMF (150 mL) was stirred at room temperature overnight. Water (500 mL) was added and the mixture was extracted with CHCl3. The organic phase was washed with water, dried and concentrated under reduced pressure. Purification by flash chromatography (hexane/EtOAc 1:1) gave [4-(methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester (8.50 g, 61%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423012B2
出典データセットuspto-grants-2008_09
ORD IDord-c7af7f81ca4e42c0a273fa448c39b0b8
出典メモuspto-grants-2008_09