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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12188Generated: October 26, 2026

Benzaldehyde → N-benzyl-serine benzyl ester

https://huagongshe.com/reaction/12188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantBenzyl L-serinate--hydrogen chloride (1/1)HCID 12930233—
SolventMethanolHCID 887—
ProductN-benzyl-serine benzyl esterHCID 5933756881%

Reaction Steps

To a mixture of L-serine-benzyl ester-HCl (2.3 g), benzaldehyde(1.05 eq.) and sodium acetate (1 eq.) in methanol was added sodium cyanoborohydride (1.0 eq.). The resulting mixture was stirred at ambient temperature for 15 hrs, then partitioned into ether and aqueous saturated sodium bicarbonate. The separated organic phase was extracted with 1M HCl (3×). Combined aqueous extracts were washed with ether, basified with aqueous 4.5M K2CO3 and extracted with ether. Combined organic extracts were washed with brine, dried over sodium sulfate and concentrated to dryness to give 2.32 g of the desired compound (waxy solid, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727985B2
Source datasetuspto-grants-2010_06
ORD IDord-d46c8f0fc93a42c984faa43c8c9ef0d6
Source noteuspto-grants-2010_06