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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570906Generated: October 25, 2026

1-(Benzyloxy)-3-chloropropan-2-one → 3-(3-Benzyloxy-2-oxo-propyl)-5-methyl-1,3,4-oxadiazol-2-one

https://huagongshe.com/reaction/570906

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Benzyloxy)-3-chloropropan-2-oneHCID 11183233—
Reactant5-Methyl-1,3,4-oxadiazol-2-one sodium saltHCID 89601806—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product3-(3-Benzyloxy-2-oxo-propyl)-5-methyl-1,3,4-oxadiazol-2-oneHCID 89602068—

Reaction Steps

To a stirred suspension of 5-methyl-1,3,4-oxadiazol-2-one sodium salt (34.6 g, 284 mmol) in DMF (200 mL) at 0° C. was added dropwise a solution of 1-benzyloxy-3-chloro-propan-2-one (56.4 g, 284 mmol) in DMF (80 mL). After completion of the addition, the reaction mixture was allowed to warm to room temperature and stirring was continued for 16 h. The obtained reaction mixture was diluted with water and brine and extracted with EtOAc. The combined organic layers were washed with water, brine, and dried (Na2SO4). After evaporation of the solvent the desired product was obtained as a brown oil. Purification by flash chromatography (25% EtOAc/heptane) furnished the desired product as a yellowish oil. 1H NMR (400 MHz, CDCl3) 2.27 (s, 3H), 4.27 (s, 2H), 4.62 (s, 2H), 4.75 (s, 2H), 7.30-7.46 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024019B2
Source datasetuspto-grants-2015_05
ORD IDord-334d5b00e2ca47678a28727b5f0aeed7
Source noteuspto-grants-2015_05