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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590577Generated: October 31, 2026

Water → 1-Methyl-4-(trifluoromethyl)pyrrole-3-carbonitrile

https://huagongshe.com/reaction/1590577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant1-methyl-4-(trifluoromethyl)-1H-pyrrole-3-carboxylic acidHCID 11788779—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-Methyl-4-(trifluoromethyl)pyrrole-3-carbonitrileHCID 21459551—

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 1-methyl-4-(trifluoromethyl)pyrrole-3-carboxylic acid (1.93 g, 0.01 mol) in acetonitrile at 40°-45° C. is treated dropwise with chlorosulfonylisocyanate (1.41 g, 0.01 mol), heated at 40° C. for 24 hours, cooled to room temperature, treated with dimethylformamide (1.46 g, 0.02 mol), heated at 40° C. for 8 hours, cooled to room temperature, stirred for 48 hours at room temperature and poured into water. The resultant mixture is extracted with ethyl acetate. The extracts are combined, washed sequentially with water and brine, dried (MgSO4) and concentrated in vacuo to afford an oily solid residue. The residue is taken up ethyl acetate, washed with 1% aqueous sodium hydroxide, dried (MgSO4) and concentrated in vacuo to give a yellow oil residue. Kugelrohr distilllation at 100°-110° C./2 mm Hg yields the title product as a white solid, 0.95 g (54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05204332
Source datasetuspto-grants-1993_04
ORD IDord-315281094e7643d5919ed6489f56abb7
Source noteuspto-grants-1993_04