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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236875Generated: October 26, 2026

Carbon Dioxide → 2-Hydroxy-1-phenyl-1-propanone

https://huagongshe.com/reaction/236875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant2-BromopropiophenoneHCID 16452—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium FormateHCID 2723810—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-Hydroxy-1-phenyl-1-propanoneHCID 10112198%

Reaction Steps

There was added 10.08 parts of sodium bicarbonate and about 60 parts of water to a mixture of 21.3 parts of α-bromopropiophenone, 6.8 parts of sodium formate and about 90 parts of acetonitrile. The resulting mixture was stirred vigorously for 48 hours at 65° C. during which time carbon dioxide evolved. After cooling, the acetonitrile solution was separated from the aqueous layer and evaporated to dryness. The residue was dissolved into chloroform which was extracted once with water, dried over sodium sulfate, and evaporated to produce analytically pure (>98%) α-hydroxypropiophenone. The yield of this isolated product was 77.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04158094
Source datasetuspto-grants-1979_06
ORD IDord-d494b997ee4a4071bf5ea7d6d61be2ab
Source noteuspto-grants-1979_06