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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131981Erstellt: 24. Oktober 2026

Pentane → 2-Cyclopentanecarbonylaniline

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPentaneHCID 8003—
Eduktt-Butyl carbanilateHCID 137930—
EduktN-methoxy-N-methylcyclopentanecarboxamideHCID 11147854—
EduktHCID 178418306HCID 178418306—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-CyclopentanecarbonylanilineHCID 1362510287,8%

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384967B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-6b79721c29714221aa9315c5d96124f7
Quellennotizuspto-grants-2008_06