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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37332Generated: October 25, 2026

Water → 1,3-Bis(2-chlorothiophenoyl)Benzene

https://huagongshe.com/reaction/37332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-ChlorothiopheneHCID 7299—
ReactantIsophthaloyl chlorideHCID 7451—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon DisulfideHCID 6348—
Product1,3-Bis(2-chlorothiophenoyl)BenzeneHCID 6778400475%

Reaction Steps

A solution of 2-chlorothiophene (0.128 mol) in 20 mL of carbon disulfide was added to a stirred suspension of isophthaloyl chloride (0.064 mol) and anhydrous aluminum chloride (0.1408 mol) in 100 mL of carbon disulfide. The reaction mixture was heated to reflux, stirred under nitrogen for 3 hours, and poured into 300 mL of water. The organic layer was separated immediately, then washed twice with 3.00 mL of 10% NaOH, twice with 300 mL of 5% HCl, and once with 500 mL of water. The product was recrystallized twice from ethyl acetate to form light yellow crystals in a 75% yield. Purity was determined by GC to be greater than 99.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420224
Source datasetuspto-grants-1995_05
ORD IDord-9e5555306d5d4ec291cd6d21577f16ab
Source noteuspto-grants-1995_05