HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472149Generated: October 26, 2026
Oxalyl chloride → 4-Hydroxybenzene-1-sulfonyl chloride
https://huagongshe.com/reaction/472149
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2060026-75-5 | HCID 86590832 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Hydroxybenzene-1-sulfonyl chloride | HCID 11424093 | 100% |
Reaction Steps
A solution of 7 g (30 mmol) of the sodium salt of 4-hydroxybenzenesulfonic acid dihydrate in 40 ml of dimethylformamide is added dropwise to a solution of 15.5 ml (181 mmol) of oxalyl chloride in 120 ml of dichloromethane cooled to −30° C. The reaction medium is slowly brought back to ambient temperature and then stirred at ambient temperature for 18 h. After the addition of 200 ml of ice, the reaction medium is extracted with ethyl acetate. The organic phase is washed with water and with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and concentrated. 6.2 g (100%) of 4-hydroxybenzenesulfonyl chloride are obtained in the form of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633196B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-8e037c33dee74eb4adbf3e9daa23da5a |
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| Source note | uspto-grants-2014_01 |
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