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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386246Generated: October 31, 2026

Benzaldehyde → HCID 67269069, compound

https://huagongshe.com/reaction/2386246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
ReactantD-ThreonineHCID 69435—
ReactantSodium borohydrideHCID 4311764—
SolventSodium HydroxideHCID 14798—
ProductHCID 67269069HCID 6726906913.2%

Reaction Steps

To (2R,3S)-2-amino-3-hydroxybutanoic acid (14.7 g, 123 mol) in NaOH (50%, 70 mL) was added benzaldehyde (14 mL, 123 mmol). The white slurry was stirred at room temperature for 18 h and then cooled to 0° C. NaBH4 (675 mg, 17.9 mmol) was added in two portions over 10 minutes Cooling bath was removed and the thick slurry was stirred at room temperature for 40 minutes and addition NaBH4 (659 mg, 17.4 mmol) was added and stirred at 0° C. for 40 minutes Benzaldehyde (10 mL, 99 mmol) was added, cooled to 0° C. and additional NaBH4 (700 mg, 18.5 mmol) was added. After 5 minutes warmed up to room temperature and stirred for 2 hour. The reaction mixture was acidified with HCl (conc.) to pH of (about 3) and then filtered precipitate, washed with cold water and dried to give (2R,3S)-2-(benzylamino)-3-hydroxybutanoic acid (3.4 g, 13.2%) of white solid. MS [M+H] found 210.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268819B2
Source datasetuspto-grants-2012_09
ORD IDord-2d3afa1785be4806af88397d1a108bc3
Source noteuspto-grants-2012_09