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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167768Generated: October 31, 2026

Thionyl Chloride → Methyl 4-aminocyclohexanecarboxylate

https://huagongshe.com/reaction/2167768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-Aminocyclohexanecarboxylic acidHCID 171560—
ReactantSodium BicarbonateHCID 516892—
SolventMethanolHCID 887—
ProductMethyl 4-aminocyclohexanecarboxylateHCID 422580—

Reaction Steps

Thionyl chloride (4.15 g, 34.92) was added to a cold (0° C.) stirred solution of 4-aminocyclohexane carboxylic acid (1 g, 6.98 mmol) in MeOH (10 mL). The reaction mixture was stirred under reflux conditions for 12-16 h. The reaction mixture was then concentrated under reduced pressure. The residue obtained was diluted with ice cold water, basified with aqueous sodium bicarbonate solution and extracted with DCM. The DCM layer was washed with water followed by brine solution, dried over anhydrous sodium sulphate and concentrated under reduced pressure to afford 650 mg of the title compound as a brown liquid. MS (ESI): m/z 158 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045479B2
Source datasetuspto-grants-2015_06
ORD IDord-b29df29fc7ff4b46a32d6fa333e81187
Source noteuspto-grants-2015_06