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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118862Generated: November 2, 2026

Benzoyl chloride → HCID 86741278, compound

https://huagongshe.com/reaction/2118862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodiumHCID 5360545—
ReactantHCID 136016126HCID 136016126—
SolventAcetoneHCID 180—
ProductHCID 86741278HCID 86741278—

Reaction Steps

A slight excess of benzoyl chloride was added to a suspension of the sodium salt of 5-(2,4-dimethylnaphth-1-yl)-2-[1-(ethoxyimino)butyl]-3-hydroxycyclohex-2-en-1-one (0.34 g) in acetone (20 ml) and the mixture was stirred at room temperature for 12 hr. The mixture was filtered, the filtrate was evaporated and the residue was purified by column chromatography overe silica with dichloromethane elution to give 3-benzoyloxy-5-(2,4-dimethylnaphth-1-yl)-2-[1-(ethoxyimino)butyl]cyclohex-2-en-1-one as a pale yellow oil. The product was characterized by proton nuclear magnetic resonance spectroscopy and the spectroscopic data is recorded in Table 4, Example 10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04680400
Source datasetuspto-grants-1987_07
ORD IDord-b0735871f4db48bf91086fdb7f75bedd
Source noteuspto-grants-1987_07