Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872350Generated: November 2, 2026

Benzaldehyde → 3-(Benzylamino)propanol

https://huagongshe.com/reaction/1872350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantTrimethyl orthoformateHCID 9005—
Reactant3-Amino-1-propanolHCID 9086—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3-(Benzylamino)propanolHCID 7844893%

Reaction Steps

To a solution of benzaldehyde (10 g, 94.23 mmol) and trimethylorthoformate (15.5 mL, 141 mmol ) in MeOH (300 mL) was added dropwise 3-amino-1-propanol (7.21 ml, 94.23 mmol) at room temperature. The reaction was allowed to stir at room temperature for 5 hours followed by cooling to 0° C. in an ice bath. Sodium borohydride (3.56 g, 94.23 mmol) was added in two portions and when the bubbling stopped the solvent was evaporated. The resulting residue was partitioned between ethyl acetate (75 mL) and water (75 ml). The aqueous layer was extracted twice with ethyl acetate (75 mL). The ethyl acetate extracts were collected and washed twice with Brine (50 mL), dried over MgSO4, filtered, and concentrated. Drying afforded 14.42 g (93%) of the compound which was used in the next step of synthesis without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107482
Source datasetuspto-grants-2000_08
ORD IDord-20760d5e90da458fb537098f8fef0df3
Source noteuspto-grants-2000_08