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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921666Generated: October 26, 2026

N-Methylcyclohexylamine → N-cyclohexyl-N-methyl-gamma-aminobutyric acid ethyl ester

https://huagongshe.com/reaction/1921666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantEthyl 4-bromobutyrateHCID 76300—
SolventEthanolHCID 702—
ProductN-cyclohexyl-N-methyl-gamma-aminobutyric acid ethyl esterHCID 6749351790.1%

Reaction Steps

10 g of 4-bromobutyric acid ethyl ester and 15 g of N-cyclohexyl-N-methylamine were added to 40 mL of ethanol, and the mixture was heated to reflux for 2 hours. After air-cooling, the mixture was concentrated under reduced pressure and extracted with 200 mL of ethyl acetate. The extracted material was washed with purified water, dried with magnesium sulfate, and then concentrated. The obtained residue was distilled under reduced pressure to give 10.5 g of N-cyclohexyl-N-methyl-gamma-aminobutyric acid ethyl ester. The obtained N-cyclohexyl-N-methyl-gamma-aminobutyric acid ethyl ester was added to a sodium hydroxide solution (2.4 g of sodium hydroxide/100 mL of purified water), and THF was added thereto until the mixture became homogeneous. After stirring at room temperature for 3 hours, the mixture was neutralized with DOWEX50W [H+ form] and concentrated under reduced pressure. The obtained residue was recrystallized to give 5.2 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173705B2
Source datasetuspto-grants-2012_05
ORD IDord-c25ed5548a08491982eb43d32fab1c60
Source noteuspto-grants-2012_05