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HRID 560031作成日:2026年10月25日

Pentane → (2-Amino-5-methyl-phenyl)-cyclopropyl-methanone

https://huagongshe.com/reaction/560031

反応式

関与物質

役割名称HCID仕込み量
反応物PentaneHCID 8003—
反応物Tert-butyl p-tolylcarbamateHCID 4935486—
反応物N-Methoxy-N-methylcyclopropanecarboxamideHCID 15643267—
反応物HCID 178418306HCID 178418306—
溶媒Diethyl EtherHCID 3283—
生成物(2-Amino-5-methyl-phenyl)-cyclopropyl-methanoneHCID 1534638195.1%

反応条件

温度-10 °C

反応手順

To a stirred solution of p-tolyl-carbamic acid tert-butyl ester (1.0 g, 4.8 mmol) in Et2O (10 mL) under a nitrogen atmosphere was added dropwise a 1.7 M solution of t-BuLi in pentan (6.5 mL, 11.1 mmol) over a 10-min period at −20° C. The mixture was stirred at −10° C. for 2.5 h and then cyclopropanecarboxylic acid methoxy-methyl-amide (0.92 g, 6.3 mmol) was added over 5 min. The mixture was allowed to warm to room temperature and stirred for further 1 h before it was quenched with aqueous NH4Cl. The organic phase was isolated and the aqueous phase was extracted with CH2Cl2, and the combined organic phases were dried and concentrated in vacuo. The crude material was dissolved CH2Cl2 (15 mL) and TFA (15 mL) and stirred at room temperature for 3 h. The reaction mixture was evaporated in vacuo, and added aqueous NaHCO3 to pH 7 and extracted with CH2Cl2. The combined organic phases were dried and concentrated in vacuo to give 0.80 g crude (2-amino-5-methyl-phenyl)-cyclopropyl-methanone as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063081B2
出典データセットuspto-grants-2011_11
ORD IDord-071a1dbd861f4554a344dd921e79eaca
出典メモuspto-grants-2011_11