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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367548Generated: October 30, 2026

Benzaldehyde → (R)(-)-2-Benzylamino-1-butanol

https://huagongshe.com/reaction/2367548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-1-butanol, (-)-HCID 2723856—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(R)(-)-2-Benzylamino-1-butanolHCID 927306108.6%

Reaction Steps

To (R)-(−)-2-amino-1-butanol (5 g, 56.1 mmol) in CH3OH (120 mL) was added benzaldehyde (6.24 mL, 61.7 mmol), and the reaction mixture was stirred under nitrogen for 15 minutes. The mixture was then cooled in an ice bath and sodium borohydride (2.33 g, 61.7 mmol) was added portionwise. The mixture was stirred in the ice bath for 1.5 hours. NaOH (6 N, 25 mL) was added and the mixture was concentrated. The resulting residue was taken up in 100 mL H2O and extracted with Et2O (2×). The organics were combined, dried over Na2SO4 and concentrated to afford the title compound (10.92 g) as a fluffy white solid. LC-MS (ES) m/z=180 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697685B2
Source datasetuspto-grants-2014_04
ORD IDord-7f20c51336c14bdd9cf8794cc468f408
Source noteuspto-grants-2014_04