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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896265Generated: October 31, 2026

Methanol → methyl (1S,3S)-3-aminocyclohexane-1-carboxylate

https://huagongshe.com/reaction/1896265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant(1S,3S)-3-Aminocyclohexanecarboxylic acidHCID 7005077—
Productmethyl (1S,3S)-3-aminocyclohexane-1-carboxylateHCID 6707043190.9%

Reaction Conditions

Temperature65 °C

Reaction Steps

Thionyl chloride (0.6 ml) was added to a solution of trans-3-amino-cyclohexane carboxylic acid (0.5 g, 2.8 mmol) in MeOH (20 ml) at 0° C. The reaction mixture was heated to 65° C. and concentrated in vacuum. The resulting residue was partitioned between saturated sodium bicarbonate (10 ml) and extracted with ethyl acetate. The combined organic layer was washed with brine solution, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum to afford 400 mg (90.9%) of trans-methyl 3-aminocyclohexanecarboxylate as colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518948B2
Source datasetuspto-grants-2013_08
ORD IDord-ecfa4c057f5a4e3cbb41df5c5a22fa50
Source noteuspto-grants-2013_08