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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866685Generated: October 30, 2026

Phenylacetone → HCID 6512704, compound

https://huagongshe.com/reaction/866685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetoneHCID 7678—
ReactantEthyl formateHCID 8025—
ReactantSodium ethoxideHCID 2723922—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 6512704HCID 6512704—

Reaction Steps

Phenylacetone (Aldrich Chem. Co. 13,538-0; Beilstein 7, 303), XXVIa (101 g, 0.75 mol) was combined with 100 g (1.35 mol) of ethyl formate and added all at once to a suspension of 50 g (0.75 mol) of sodium ethoxide in 500 ml of THF. After 3 hours at room temperature the brown solution was diluted with 400 ml of H2O. Following extraction with benzene to remove unreacted starting material, the aqueous phase was acidified with dilute HCl. The product was extracted with benzene, washed with H2O, dried over MgSO4, and concentrated to give an oil. Distillation gave 39 g (0.24 mol) of (Z)-1-hydroxymethylene-1-phenylacetone, XXVIIa, as a colorless oil, bp 65°-69° C (0.3 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04100353
Source datasetuspto-grants-1978_07
ORD IDord-0f80dc7eff224b53866e31e1ef2d39ed
Source noteuspto-grants-1978_07