HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417246Generated: October 31, 2026
HCID 9837522, compound → HCID 10522547, compound
https://huagongshe.com/reaction/1417246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 9837522 | HCID 9837522 | — |
| Reactant | 2-Bromo-1-(4-hydroxy-3-methylphenyl)ethanone | HCID 11218449 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10522547 | HCID 10522547 | 24.8% |
Reaction Steps
A solution of 26 g of 4-toluenesulfonyl-thiourea in 225 ml of ethanol was treated with 25.9 g of 2-bromo-1-(4-hydroxy-3-methyl-phenyl)-ethanone, left to stand at room temperature for 3 days and then boiled for a brief period. The reaction mixture was evaporated to dryness in a vacuum and subsequently partitioned between water and ethyl acetate. The aqueous phase was extracted once with ethyl acetate, the organic phases were combined, dried with sodium sulphate and concentrated. The residue was chromatographed on 500 g of Kieselgel 60 with ethyl acetate/hexane (1:1) as the eluent. The product-containing fractions were concentrated and, after recrystallization from 50% ethanol, yielded 10.1 g of N-[4-(4-hydroxy-3-methyl-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamide as colourless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05877193 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-0dc488b3c19f40af812c3560a206ebca |
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| Source note | uspto-grants-1999_03 |
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