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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526718Generated: October 25, 2026

Potassium Formate → N-benzyl-4-hydroxy-3-oxobutanamide

https://huagongshe.com/reaction/526718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FormateHCID 2735122—
ReactantN-benzyl-4-bromo-3-oxobutanamideHCID 71502812—
SolventMethanolHCID 887—
ProductN-benzyl-4-hydroxy-3-oxobutanamideHCID 7150281354.6%

Reaction Conditions

Temperature-10 °C

Reaction Steps

N-benzyl-4-bromo-3-oxobutanamide (compound B 50 g, 185.1 mmol) was dissolved in methanol (400 ml), and potassium formate (31.14 g, 370.2 mmol) was added. The resulting mixture was heated under reflux for 2 hours. Methanol was removed by distillation under reduced pressure; the residue was taken up into ethyl acetate (250 ml) under reflux, filtered hot, the filter cake washed with warm ethyl acetate (100 ml). The combined filtrate was cooled to −10° C., aged for 1.5 hours. The precipitate was collected, washed twice with cold ethyl acetate (2×25 ml), dried to give N-benzyl-4-hydroxy-3-oxobutanamide (18.2 g, 101 mmol, 38.8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346751B2
Source datasetuspto-grants-2016_05
ORD IDord-75d1eb007b04441f8953c1e8edbc0291
Source noteuspto-grants-2016_05