Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423049Generated: October 26, 2026

Methanol → 3-Amino-3-(4-chlorophenyl)propan-1-ol

https://huagongshe.com/reaction/423049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-Amino-3-(4-chlorophenyl)propanoic acidHCID 344176—
SolventTetrahydrofuranHCID 8028—
Product3-Amino-3-(4-chlorophenyl)propan-1-olHCID 1703943556.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Borane-tetrahydrofuran complex (94.0 mL, 93.92 mmol) was added dropwise to a stirred suspension of 3-amino-3-(4-chlorophenyl)propionic acid (2.50 g, 12.52 mmol) in THF (75 mL) at 0° C. over a period of 20 minutes under nitrogen. The resulting suspension was stirred at 0° C. for 30 minutes then at 22° C. for 5 hours. The reaction mixture was added portionwise to methanol (500 mL). The mixture was concentrated, redissolved in methanol (250 mL) and reconcentrated (this process was repeated three times). The residue was dissolved in DCM (200 mL) and washed with 1N NaOH (150 mL). The aqueous layer was extracted with DCM (5×100 mL) and the extracts combined with the organic layer. The combined organics were washed with saturated brine (2×150 mL), dried over MgSO4 and concentrated to afford a white semi-solid. The crude product was purified by flash silica chromatography, elution gradient 5 to 7% (10:1 MeOH/conc. NH3 (aq)) in DCM. Pure fractions were evaporated to dryness to afford 3-amino-3-(4-chlorophenyl)propan-1-ol (1.320 g, 56.8%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101623B2
Source datasetuspto-grants-2012_01
ORD IDord-86bbb29a1ac042cd89b6e1fee70c496a
Source noteuspto-grants-2012_01