Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983880Generated: November 2, 2026

2,3-Dichloropropene → 5-Bromo-2-methyl-1-benzothiophene

https://huagongshe.com/reaction/1983880

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichloropropeneHCID 6565—
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromothiophenolHCID 66049—
SolventAcetoneHCID 180—
Product5-Bromo-2-methyl-1-benzothiopheneHCID 1366303598%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 4-bromothiophenol (5.0 g, 26.4 mmol), 2,3-dichloro-1-propene (2.6 g, 23.8 mmol) and potassium carbonate (4.4 g, 31.7 mmol) in acetone (20 ml) was stirred at 55° C. for 6 hours. After cooling to room temperature, acetone was removed under vacuum and the residue was taken into water and extracted with ethyl acetate twice. The combined organic layers were washed with 1 M sodium hydroxide, water and brine, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. Diethylaniline (30 ml) was added to the residue and the resulting mixture was stirred at 185° C. for 15 hours. Ethyl acetate was added to the cooled mixture and diethylaniline was removed by washing with 1 M HCl four times. The organic layer was dried over sodium carbonate to give 5-bromo-2-methylbenzothiophene (5.3 g, 88%, 95.1% AUC GC): 1H NMR (300 MHz, CDCl3) δ 7.70 (s, 1H), 7.52 (d, J=8.7 Hz, 1H), 7.26 (dd, J=8.7, 1.8 Hz, 1H), 6.83 (s, 1H), 2.51 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541357B2
Source datasetuspto-grants-2009_06
ORD IDord-cc8623a0d3674c41b99e49bc6ded594e
Source noteuspto-grants-2009_06