HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374045Generated: October 31, 2026
Water → 4-[4-(2,5-Dichlorobenzoyl)phenoxy]benzene-1-sulfonyl chloride
https://huagongshe.com/reaction/1374045
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 4-[4-(2,5-Dichlorobenzoyl)phenoxy]benzene sulfonic acid | HCID 17965292 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sulfolane | HCID 31347 | — |
| Product | 4-[4-(2,5-Dichlorobenzoyl)phenoxy]benzene-1-sulfonyl chloride | HCID 17965291 | 87% |
Reaction Steps
To 215 g (about 400 mmol) of the crude crystal of A-SO3Na, 300 mL of acetonitrile and 200 mL of sulfolane as a solvent were added, and further phosphoryl trichloride (245.3 g, 1.6 mole) was added and then reacted at 70° C. to obtain a reaction mixture. Further, 5 mL of N,N-dimethyl acetoamide was added thereto and the resulting yellow suspension was stirred at 71 to 73° C. for 40 min and then cooled to 3° C. To the suspension, 1 L of cool water was added at a rate such that the temperature of the reaction system was not over 10° C. The resulting precipitate was collected, washed with cool water and re-crystallized with 350 mL of toluene to obtain 153 g of the aimed white crystalline A-SO2Cl having a melting point of from 130.5 to 131.5° C. (yield: 87% on the basis of A). The IR spectrum is shown in FIG. 4 and the NMR spectrum is shown in FIGS. 5 and 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163988B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-54bb713ec685444fb35ec4e85ddd523b |
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| Source note | uspto-grants-2007_01 |
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