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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131981생성일: 2026년 10월 24일

Pentane → 2-Cyclopentanecarbonylaniline

https://huagongshe.com/ko/reaction/131981

반응식

참여 물질

역할이름HCID투입량
반응물PentaneHCID 8003—
반응물t-Butyl carbanilateHCID 137930—
반응물N-methoxy-N-methylcyclopentanecarboxamideHCID 11147854—
반응물HCID 178418306HCID 178418306—
용매Diethyl EtherHCID 3283—
생성물2-CyclopentanecarbonylanilineHCID 1362510287.8%

반응 조건

온도-10 °C

반응 단계

To a stirred solution of phenyl-carbamic acid tert-butyl ester (1.2 g, 6.2 mmol) in Et2O (12 mL) under a nitrogen atmosphere was added dropwise a 1.7 M solution of t-BuLi in pentan (8.4 mL, 14.3 mmol) over a 10-min period at −20° C. The mixture was stirred at −10° C. for 2.5 h and then cyclopentanecarboxylic acid methoxy-methyl-amide (1.07 g, 6.8 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 (18 mL) and TFA (6 mL) and stirred at room temperature for 2 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 1.03 g (68%) of (2-amino-phenyl)-cyclopentyl-methanone as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384967B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-6b79721c29714221aa9315c5d96124f7
출처 메모uspto-grants-2008_06