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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522538Generated: November 2, 2026

Benzenesulfonyl chloride → 5-Bromo-2-butylbenzofuran

https://huagongshe.com/reaction/522538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant2-(4-Bromo-2-formylphenoxy)hexanoic acidHCID 22057826—
ReactantEthyl acetate methylcyclohexaneHCID 66985183—
SolventTolueneHCID 1140—
Product5-Bromo-2-butylbenzofuranHCID 56926023—

Reaction Conditions

Temperature80 °C

Reaction Steps

25.8 ml of benzenesulfonyl chloride (0.202 mol; 1.4 equivalents) and 40 ml of toluene are placed in an equipped reactor and the mixture is stirred at 80° C. 65 ml of anhydrous triethylamine (0.47 mol) and then 45.2 g of 2-(4-bromo-2-formylphenoxy)hexanoic acid (compound VIII) (0.144 mol) dissolved in 250 ml of toluene are then added slowly at 80° C. The reaction progress is monitored by TLC (eluent: 80/20 methylcyclohexane/ethyl acetate; Rf of compound VIII=0.08; Rf of the desired compound IX=0.80).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334254B2
Source datasetuspto-grants-2016_05
ORD IDord-aaf4388929724f84b3113c0b1d7d133a
Source noteuspto-grants-2016_05