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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913863Generated: October 27, 2026

Hydrochloric Acid → 3-Amino-1-(2-chloro-phenyl)-propan-1-ol hydrochloride

https://huagongshe.com/reaction/1913863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoraneHCID 6331—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant3-(2-Chlorophenyl)-3-hydroxypropanenitrileHCID 11975498—
SolventMethanolHCID 887—
Product3-Amino-1-(2-chloro-phenyl)-propan-1-ol hydrochlorideHCID 86762186176.1%

Reaction Conditions

Temperature75 °C

Reaction Steps

3-(2-Chloro-phenyl)-3-hydroxy-propionitrile (740 mg, 4.07 mmol) was slowly treated with a solution of borane-tetrahydrofuran complex (9 mL, 8.96 mmol, 1M in tetrahydrofuran) at 0° C. After bubbling ceased, the reaction mixture was heated to 75° C. for 2 hours and 1.1 eq of additional borane was added to drive the reaction to completion. The reaction mixture was concentrated. The white solid obtained was treated with methanol (14 mL), followed by hydrogen chloride (2M in diethyl ether, 14 mL). The resulting mixture was heated to reflux for 2 hours, allowed to cool to ambient temperature and then concentrated at reduced pressure. To the residue was added aqueous hydrochloric acid (10 mL, 1 N) followed by diethyl ether (20 mL). The aqueous layers were separated and concentrated at reduced pressure and dried to give the product as a white solid (796 mg, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609849B1
Source datasetuspto-grants-2013_12
ORD IDord-8f57ebd270e84c4d953e39518ff6d135
Source noteuspto-grants-2013_12