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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sulfolane | HCID 31347 | — |
| Reactant | 4-[4-(2,5-Dichlorobenzoyl)phenoxy]benzene sulfonic acid sodium salt | HCID 23709805 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-[4-(2,5-Dichlorobenzoyl)phenoxy]benzene-1-sulfonyl chloride | HCID 17965291 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687187B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-ae7d72329dc54d0db9bd68fd2f453437 |
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| Source note | uspto-grants-2010_03 |
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