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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417246Generated: October 31, 2026

HCID 9837522, compound → HCID 10522547, compound

https://huagongshe.com/reaction/1417246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 9837522HCID 9837522—
Reactant2-Bromo-1-(4-hydroxy-3-methylphenyl)ethanoneHCID 11218449—
SolventEthanolHCID 702—
ProductHCID 10522547HCID 1052254724.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877193
Source datasetuspto-grants-1999_03
ORD IDord-0dc488b3c19f40af812c3560a206ebca
Source noteuspto-grants-1999_03