Pentane → 2-Cyclopentanecarbonylaniline

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.

1. temperatureto warm to room temperature
2. stirringstirred for further 1 h before it
3. customwas quenched with aqueous NH4Cl
4. customThe organic phase was isolated
5. extractionthe aqueous phase was extracted with CH2Cl2
6. customthe combined organic phases were dried
7. concentrationconcentrated in vacuo
8. dissolutionThe crude material was dissolved CH2Cl2 (18 mL) and TFA (6 mL)
9. stirringstirred at room temperature for 2 h
10. customThe reaction mixture was evaporated in vacuo
11. additionadded aqueous NaHCO3 to pH 7
12. extractionextracted with CH2Cl2
13. customThe combined organic phases were dried
14. concentrationconcentrated in vacuo

ORDレコード

ord-6b79721c29714221aa9315c5d96124f7

出典データセット

uspto-grants-2008_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07384967B2