Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846714Generated: October 31, 2026

4-Chlorobenzoyl chloride → HCID 19883675, compound

https://huagongshe.com/reaction/846714

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
Reactant7-Phenyl-1-heptyl chlorideHCID 522410—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventNitrobenzeneHCID 7416—
ProductHCID 19883675HCID 1988367574.4%

Reaction Steps

1.07 g of 7-chloroheptylbenzene and 0.89 g of 4-chlorobenzoyl chloride were dissolved in 10 ml of nitrobenzene and treated with 0.82 g of aluminium chloride under argon and while cooling with ice. The mixture was then stirred at room temperature for 18 hours, taken up in 100 ml of ice-cold 2N hydrochloric acid solution and extracted three times with 50 ml of ether each time. The organic phases were washed with 50 ml of a 10 percent sodium bicarbonate solution and 50 ml of a saturated sodium chloride solution, dried over magnesium sulphate and concentrated. The nitrobenzene was removed by distillation at 80°-100° C. and 20 Pa. By distillation at 240°-250° C. and about 13.4 Pa there were obtained 1.32 g (74%) of 4-chloro-4'-(7-chloroheptyl)benzophenone as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137920
Source datasetuspto-grants-1992_08
ORD IDord-186bfe639a67481aae1a7daa1a88b54e
Source noteuspto-grants-1992_08