Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176903Generated: October 30, 2026

Acetic Anhydride → HCID 131730828, compound

https://huagongshe.com/reaction/2176903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 67070431HCID 67070431—
SolventPyridineHCID 1049—
ProductHCID 131730828HCID 13173082869.2%

Reaction Steps

Acetic anhydride (1.20 ml, 12.7 mmol) was added to a solution of trans-methyl 3-aminocyclohexane-carboxylate (0.40 g, 2.54 mmol) in pyridine (10 ml) at 0° C. The reaction mixture was warmed to room temperature and stirred for 1 h. The volatiles were removed in vacuum, the resulting residue was dissolved in DCM and washed with saturated sodium bicarbonate solution followed by brine solution (10 ml). After drying over anhydrous sodium sulfate and filtration the filtrate was concentrated under vacuum to afford 350 mg (69.0%) of trans-methyl 3-acetamidocyclohexanecarboxylate as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067888B2
Source datasetuspto-grants-2015_06
ORD IDord-7a0fc787bc5b405f87f3a13c52d1638a
Source noteuspto-grants-2015_06