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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423039Generated: October 29, 2026

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

https://huagongshe.com/reaction/423039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl (S)-3-((tert-butoxycarbonyl)amino)-3-(4-chlorophenyl)propanoateHCID 57750406—
SolventDichloromethaneHCID 6344—
Product(S)-Methyl 3-amino-3-(4-chlorophenyl)propanoateHCID 2400961118.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

Hydrochloric acid (4.0M in 1,4 Dioxane) (4.18 mL, 16.73 mmol) was added in one portion to (S)-methyl 3-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)propanoate (Intermediate 19) (1.05 g, 3.35 mmol) in DCM (20 mL) at 20° C. The resulting solution was stirred at 20° C. for 5 hours. The reaction mixture was evaporated to give (S)-methyl 3-amino-3-(4-chlorophenyl)propanoate (hydrochloride) (0.850 g, 102%) as a white solid. 1H NMR (399.9 MHz, DMSO-d6) δ 2.98-3.04 (1H, m), 3.16-3.21 (1H, m), 3.58 (3H, s), 4.62-4.66 (1H, m), 7.50-7.52 (2H, m), 7.57-7.59 (2H, m), 8.66 (3H, s). m/z (ESI+) (M+H)+=214; HPLC tR=1.71 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101623B2
Source datasetuspto-grants-2012_01
ORD IDord-23c3376aa8f148c09678f1902f74b584
Source noteuspto-grants-2012_01