Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065178Generated: October 25, 2026

Boron trifluoride → 1-tert-Butyl-4-(3-chloro-2-methylpropyl)benzene

https://huagongshe.com/reaction/1065178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
Reactanttert-BUTYL CHLORIDEHCID 10486—
Reactant(3-Chloro-2-methylpropyl)benzeneHCID 13510156—
SolventWaterHCID 962—
Product1-tert-Butyl-4-(3-chloro-2-methylpropyl)benzeneHCID 13251817—
Product(3-Chloro-2-methylpropyl)benzeneHCID 13510156—

Reaction Steps

BF3 is passed for 30 minutes into a mixture of 84 parts by weight of 2-methyl-3-phenyl-propyl chloride and 50 ml of BF3 ·2H2O at room temperature. 56 parts by weight of tert.-butyl chloride are then added dropwise at room temperature. The mixture is refluxed for 4 hours and is then allowed to cool; the crude product is introduced into water and extracted with chloroform. The organic phase is separated off, washed with water, dried over Na2CO3 and distilled. 30 parts by weight of 2-methyl-3-phenyl-propyl chloride, boiling point 105° C./16 mm Hg, and 45 parts by weight of 2-methyl-3-(p-tert.-butylphenyl)-propyl chloride, boiling point 80° C.-81° C./0.02 mm Hg, are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04328380
Source datasetuspto-grants-1982_05
ORD IDord-62ed638def68417c87c569adbce2f41d
Source noteuspto-grants-1982_05