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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049864Generated: October 27, 2026

Chlorosulfonic acid → 5-Acetylamino-4-carbamoyl-3-methyl-thiophene-2-sulfonyl chloride

https://huagongshe.com/reaction/1049864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant2-Acetylamino-4-methylthiophene-3-carboxylic acid amideHCID 2807708—
Product5-Acetylamino-4-carbamoyl-3-methyl-thiophene-2-sulfonyl chlorideHCID 117703965—

Reaction Conditions

Temperature40 °C

Reaction Steps

Neat ClSO3H (6.7 mL, 100 mmol) is cooled to 0° C. 2-acetylamino-4-methyl-thiophene-3-carboxylic acid amide (1.98 g, 10 mmol) is added in portions over a period of 15 min, and the mixture is stirred at 40° C. for 3 h. The mixture is cooled down to room temperature and poured slowly onto ice cold water. The resulting suspension is washed twice with EtOAc, the combined organic fractions are dried over MgSO4, filtered and evaporated to yield the desired product which is used as such.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382254B2
Source datasetuspto-grants-2016_07
ORD IDord-61d5b89f45a94d9bb3b2fe2000a3cf60
Source noteuspto-grants-2016_07