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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281477Generated: November 2, 2026

5-(Bromoacetyl)-2-(phenylmethoxy)benzamide → 2-(Benzyloxy)-5-(2-oxiranyl)benzamide

https://huagongshe.com/reaction/1281477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Bromoacetyl)-2-(phenylmethoxy)benzamideHCID 3018338—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product2-(Benzyloxy)-5-(2-oxiranyl)benzamideHCID 990350696.2%

Reaction Steps

2-(Benzyloxy)-5-(2-bromoacetyl)benzamide (11.3 g, 32.30 mmol) was dissolved in anhydrous tetrahydrofuran (250 mL) and cooled in an ice bath. The solution was diluted with ethanol (250 mL). Sodium borohydride (1.2 g, 32.3 mmol) was added in three portions. Following addition the solvent was removed in vacuo and the residue partitioned between water and ethyl acetate. The organic layer was washed with water, brine, and dried over anhydrous magnesium sulfate. The solution was filtered and the solvent evaporated to dryness in vacuo to yield crude title compound (1 0.88 g, 31.06 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451814B1
Source datasetuspto-grants-2002_09
ORD IDord-412c3d214f844e14a6a576ed302311c6
Source noteuspto-grants-2002_09