Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382170Generated: October 31, 2026

Benzoyl chloride → HCID 73771260, compound

https://huagongshe.com/reaction/1382170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 136082425HCID 136082425—
SolventAcetoneHCID 180—
ProductHCID 73771260HCID 7377126074.2%

Reaction Steps

Aqueous 1% sodium hydroxide solution (6.1 ml) was added to a solution of 2-[1-(ethoxyimino)propyl]-3-hydroxy-5-(2,4,6-trimethoxyphenyl)cyclohex-2-en-1-one (0.52 g; 1.40 mmole) in acetone (25 ml). The mixture was stirred at room temperature for a period of 5 minutes and then benzoyl chloride (0.21 g) was added dropwise. The mixture was stirred for a further period of 15 minutes and then the solvent was removed by evaporation under reduced pressure. The product was purified by chromatography over silica gel (eluant dichloromethane) to give 3-benzoyloxy-2-[1-(ethoxyimino)propyl]-5-(2,4,6-trimethoxyphenyl)cyclohex-2-en-1-one (0.50 g; 73.9%) as a pale yellow solid, mp 139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04806141
Source datasetuspto-grants-1989_02
ORD IDord-a8062140e40c4fa9ad4ff6e62c77c635
Source noteuspto-grants-1989_02