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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246027Generated: November 1, 2026

Acetonitrile → 4-[4-(2,5-Dichlorobenzoyl)phenoxy]benzene-1-sulfonyl chloride

https://huagongshe.com/reaction/2246027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSulfolaneHCID 31347—
Reactant4-[4-(2,5-Dichlorobenzoyl)phenoxy]benzene sulfonic acid sodium saltHCID 23709805—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product4-[4-(2,5-Dichlorobenzoyl)phenoxy]benzene-1-sulfonyl chlorideHCID 17965291—

Reaction Conditions

Temperature72 °C

Reaction Steps

Solvent (300 mL of acetonitrile and 200 mL of sulfolane) was added to 215 g (about 400 mmol) of crude crystal of A—SO3Na. Furthermore, phosphoryl trichloride (245.3 g, 1.6 mol) was added and reacted at 70° C. Furthermore, 5 mL of N,N-dimethylacetamide was added, a yellow suspension was stirred for 40 minutes at 71 to 73° C., and the reaction liquid was cooled to 3° C. 1 L of cold water was added at a rate so that the temperature of the reaction liquid did not exceed 10° C. The deposit was filtered and collected, washed with cold water, and recrystallized with 350 mL of toluene to obtain 153 of white crystal of 4-[4-(2,5-dichlorobenzoyl)phenoxy]benzene sulfonic acid chloride (A—SO3Cl). Yield depending on A was 87%. Melting point is 130.5 to 131.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687187B2
Source datasetuspto-grants-2010_03
ORD IDord-ae7d72329dc54d0db9bd68fd2f453437
Source noteuspto-grants-2010_03