Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200298Generated: November 1, 2026

Hydrochloric Acid → Methyl 3-amino-2-(4-chlorophenyl)propanoate hydrochloride

https://huagongshe.com/reaction/2200298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 3-(Boc-amino)-2-(4-chlorophenyl)propanoateHCID 66617917—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 3-amino-2-(4-chlorophenyl)propanoate hydrochlorideHCID 66617900178.2%

Reaction Steps

A solution of methyl 3-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)propanoate (451 mg, 1.44 mmol) in dioxane (6.0 mL) was treated with 4M HCl in dioxane (about 6.0 mL, 23.0 mmol) at room temperature. The mixture was stirred for 18 hours to completion, after which the reaction mixture was diluted with ether to afford a precipitate. The slurry was filtered under nitrogen to afford a white solid, which was washed with ether. The solid was dried under vacuum to afford the methyl 3-amino-2-(4-chlorophenyl)propanoate hydrochloride as a white solid (321 mg, 89%). LCMS (APCI+) m/z 214.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359340B2
Source datasetuspto-grants-2016_06
ORD IDord-944384b8d83647ae9feb1933682931a8
Source noteuspto-grants-2016_06