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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715667Generated: October 27, 2026

HCID 178472436, compound → HCID 178472435, compound

https://huagongshe.com/reaction/715667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178472436HCID 178472436—
ReactantHCID 178511567HCID 178511567—
ProductHCID 178472435HCID 178472435—

Reaction Steps

19.3 mL of concentrated hydrochloric acid (2.8 eq) was added to a solution of cis-4-aminocyclohexane carboxylic acid (10 g, 69.83 mmol) in anhydrous ethyl alcohol (250 mL). Mixture was stirred overnight at about 60° C. and then cooled to room temperature. Solvent was evaporated in vacuo. Crude material was then redissolved in acetonitrile, sonicated, and concentrated to a solid in vacuo. This acetonitrile wash was repeated three times to obtain 11.5 g of while solid (96% yield). Trans-ethyl 4-aminocyclohexanecarboxylate hydrochloride can be prepared following the same procedure using trans-4-aminocyclohexane carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187479B2
Source datasetuspto-grants-2015_11
ORD IDord-a424c350cc624310ba161085c814fd7c
Source noteuspto-grants-2015_11