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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292917Generated: November 1, 2026

Water → HCID 10737609, compound

https://huagongshe.com/reaction/2292917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThionyl ChlorideHCID 24386—
Reactant3,3,3-Trifluoro-2-hydroxy-2-methylpropanoic acidHCID 2775125—
ReactantHCID 10585340HCID 10585340—
SolventDimethylacetamideHCID 31374—
ProductHCID 10737609HCID 1073760994.8%

Reaction Steps

To a stirred, cooled (-20° C.) solution of 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid (1.62 g 10.2 mmol) in N,N-dimethylacetamide (15 mL) was rapidly added thionyl chloride (1.30 g, 10.9 mmol) and the mixture (a precipitate formed after a few minutes) stirred at -20° C. to -5° C. for 1 hour. 4-Cyano-3-phenylthiobenzenamine (1.55 g, 6.85 mmol) was then added in one portion and the mixture allowed to stir at room temperature overnight. The solution was poured into water, extracted with ethyl ether (2×100 mL); the ethereal extracts dried (MgSO4), filtered and the solvent removed in vacuo. The residue was chromatographed on 315 g of silica gel using a ethyl ether (0%, 10%, and 20%) in methylene chloride gradient. The proper fractions were combined, the solvent removed in vacuo and the residue dissolved in a mixture of 100 mL hexane and 150 mL methylene chloride. Most of the methylene chloride was distilled off as the solution was scratched to induce crystal growth. After cooling the solid was collected and dried at 85° C./0.1 mm to yield the title propanamide (2.38 g, 91%); mp 111°-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684198
Source datasetuspto-grants-1997_11
ORD IDord-f0dbd75f46d44eed94c3bea6e3ff5f95
Source noteuspto-grants-1997_11