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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515487Generated: October 29, 2026

Hydrochloric Acid → 3-{[(4-Methoxyphenyl)methyl]amino}propan-1-ol

https://huagongshe.com/reaction/515487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Amino-1-propanolHCID 9086—
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantSodium borohydrideHCID 4311764—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product3-{[(4-Methoxyphenyl)methyl]amino}propan-1-olHCID 510098142%

Reaction Steps

To a solution of 3-amino-propan-1-ol (15.0 g, 200 mmol) in methanol (300 ml) was added para-methoxybenzaldehyde (28.6 g, 210 mmol) and a few drops of acetic acid at room temperature. The mixture was stirred at room temperature for 2 hours and cooled to 0° C. After the addition of sodium borohydride (11.4 g, 300 mmol), the mixture was stirred at room temperature for another 2 hours and acidified with 3N hydrochloric acid. The biphasic mixture was stirred at room temperature for 10 minutes. The organic solvent was evaporated under reduced pressure and the residue was partitioned between water and ethyl acetate. The aqueous phase was washed with ethyl acetate and basified with 6N sodium hydroxide. Extraction with chloroform was performed and the organic phase was dried over sodium sulfate followed by concentration in vacuo to afford 3-(4-methoxy-benzylamino)-propan-1-ol as pale yellow oil (16.4 g, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108957B2
Source datasetuspto-grants-2015_08
ORD IDord-6a886eccc8d344bd925a7d6489568f0f
Source noteuspto-grants-2015_08