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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457706Generated: October 25, 2026

Sulfuryl chloride → 4-(2-Thienyl)Benzoyl Chloride

https://huagongshe.com/reaction/1457706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant4-(Thiophen-2-yl)benzoic acidHCID 736498—
Product4-(2-Thienyl)Benzoyl ChlorideHCID 2776331—

Reaction Steps

A mixture of 3 g of 4-(2-thienyl)benzoic acid and 30 ml of sulfonyl chloride is refluxed for 45 minutes and the solvent removed. The residue is dissolved in carbon tetrachloride and the solvent removed under vacuum (2-times) to give 4-(2-thienyl) benzoyl chloride. To a cooled (0° C.) solution of 2.0 g of 5,11-dihydro-10H-dibenz[b,e][1,4]diazepine and 7 ml of N,N-diisopropylethylamine in 30 ml of dichloromethane is added dropwise a solution of 3.15 g of 4-(2-thienyl)benzoyl chloride in 30 ml of dichloromethane. The mixture is stirred at room temperature for 16 hours and diluted with 50 ml of chloroform. The solution is washed with 30 ml each of water, 2N HCl, saturated NaHCO3, water and dried (Na2 SO4). The solvent is removed under vacuum and the residue (3.1 g) chromatographed on silica gel (column) with hexane-ethyl acetate (2:1) as eluent to give 1.8 g of solid, m.p. 114° C.-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849735
Source datasetuspto-grants-1998_12
ORD IDord-32a62679b2324e5b96efa9b6ba511033
Source noteuspto-grants-1998_12