HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699556Generated: October 30, 2026
Chlorosulfonic acid → HCID 18707243, compound
https://huagongshe.com/reaction/1699556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | HCID 18707166 | HCID 18707166 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 18707243 | HCID 18707243 | — |
Reaction Steps
2 ml of chlorosulfonic acid was dropwise added to 40 ml of pyridine at room temperature. The mixture was stirred at 50° C. for 12 hours. Thereto was added 0.33 g of 4-(4-hydroxyphenyl-2-(3,4-dimethoxyphenyl)thiazole. The mixture was stirred at 50° C. for 6 hours and then at room temperature overnight. The reaction mixture was concentrated to dryness under reduced pressure. The residue was mixed with water and the resulting crystals were collected by filtration. The resulting 4-(4-hydroxysulfonyloxyphenyl)-2-(3,4-dimethoxyphenyl)thiazole pyridinium salt was suspended in 3 ml of methanol. Thereto was added 5 ml of a 0.1N aqueous potassium hydroxide solution. The mixture was stirred at room temperature overnight, The reaction mixture was concentrated. The residue was dissolved in water. The solution was treated with 0.5 g of an ion exchange resin (Dowex 50Wx8), The filtrate was concentrated to obtain 0.04 g of 4-(4-hydroxysulfonyloxyphenyl)-2-(3,4-dimethoxyphenyl)thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE037556E1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-997ea165344f4108bac05403a1f225d9 |
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| Source note | uspto-grants-2002_02 |
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