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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237266Generated: October 26, 2026

Tert-Butylbenzene → 1-(4-T-Butylphenyl)-3-chloropropan-1-one

https://huagongshe.com/reaction/237266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylbenzeneHCID 7366—
Reactant3-Chloropropionyl chlorideHCID 69364—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product1-(4-T-Butylphenyl)-3-chloropropan-1-oneHCID 22228393—

Reaction Steps

To a solution of tert-butyl benzene (1.0 g, 7.5 mmol) and 3-chloropropionyl chloride (0.7 mL, 7.5 mmoL) in CH2Cl2 (20 mL) was added dropwise to a suspension of AlCl3 (1.1 g, 8.2 mmol) in CH2Cl2 (10 mL) at 0° C. The reaction was allowed to warm to rt. After 15 h, the reaction was quenched with H2O (10 mL) and extracted with CH2Cl2 (2×20 mL). The organic layers were combined and dried to give the title compound that was used without further purification (1.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642583B2
Source datasetuspto-grants-2014_02
ORD IDord-d0b465b69b154d308bdf2b1dce9959ce
Source noteuspto-grants-2014_02