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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719126Generated: November 1, 2026

Ammonia → 2-amino-1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one O-methyl-oxime

https://huagongshe.com/reaction/719126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-bromo-1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one O-methyl-oximeHCID 73852545—
SolventMethanolHCID 887—
Product2-amino-1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one O-methyl-oximeHCID 7385254645%

Reaction Conditions

Temperature0 °C

Reaction Steps

The 2-bromo-1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one O-methyl-oxime (1.16 g, 2.901 mmol) was dissolved in a solution of ammonia in methanol (30 mL, ˜7 N). The reaction flask was sealed with a Teflon stopper, and the reaction mixture was stirred at 55–60° C. for 2 d. It was cooled to 0° C. then the stopper was removed. The reaction mixture was concentrated to remove ammonia and methanol. The residue was partitioned between water and diethyl ether. The product was extracted with diethyl ether (2×20 mL). The organic layers were washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. Purification of the crude residue by flash chromatography (Biotage system, KP-Sil™ 32–63 μm, 60 Å silica gel) eluting with 50–100% ethyl acetate+0.1% triethylamine in hexanes yielded 2-amino-1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one O-methyl-oxime (423 mg, 45%) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132421B2
Source datasetuspto-grants-2006_11
ORD IDord-f9c81ba470ec4a70a52f0114d2b356eb
Source noteuspto-grants-2006_11