Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703582Generated: October 30, 2026

Sec-Butylbenzene → HCID 21328147, compound

https://huagongshe.com/reaction/1703582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSec-ButylbenzeneHCID 8680—
Reactant2-Fluorobenzoyl chlorideHCID 9808—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventHCID 178420937HCID 178420937—
ProductHCID 21328147HCID 2132814776.4%

Reaction Steps

A 3.17 g (0.02 mole) of 2-fluorobenzoic acid chloride was dissolved in 30 ml of carbon bisulfide and then, 3.99 g (0.03 mole) of anhydrous aluminum chloride was added to the solution. A 2.68 g (0.02 mole) of sec-butyl benzene was further added to the mixture with stirring and the reaction was carried out at room temperature for 18 hours. Carbon bisulfide was distilled off from the reaction mixture and water was added and the reaction product was extracted with benzene. The benzene phase was separated washed with 1N-NaOH and with water and was dried with anhydrous sodium sulfate. The solvent was distilled off to obtain a pale yellow oily product. The oily product was distilled under a reduced pressure to obtain 3.9 g of 4-sec-butyl-2'-fluorobenzophenone having a boiling point of 152° to 160° C./5 mmHg. (yield of 76.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04124726
Source datasetuspto-grants-1978_11
ORD IDord-f6e3defd9488478ba368473e8232839e
Source noteuspto-grants-1978_11