Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583218Generated: November 1, 2026

HCID 20159499, compound → HCID 21285333, compound

https://huagongshe.com/reaction/1583218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20159499HCID 20159499—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
ProductHCID 21285333HCID 21285333—

Reaction Steps

The crude 2-chloro-4-[[p-(p-hexylphenyl)benzoyl]oxy]benzaldehyde (67.1 g) obtained was dissolved in 2500 ml of acetone. 80 ml of Jones' reagent were added dropwise to this solution within 45 minutes, the mixture warming slightly. The mixture was stirred for a further 3 hours, then the precipitated inorganic material was filtered off under suction and the acetone was distilled off on a rotary evaporator. The residue was suspended in water and the suspension was suction filtered. The crude 2-chloro-4-[[p-(p-hexylphenyl)benzoyl]oxy]benzoic acid obtained was washed neutral on the suction filter with water and then, for purification, boiled up with methanol, cooled, filtered off and dried. Yield 58.5 g; m.p. 163.8°-165.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04550981
Source datasetuspto-grants-1985_11
ORD IDord-caef5078de5e4935a39e56ef5e821a57
Source noteuspto-grants-1985_11