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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372966Generated: October 30, 2026

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

https://huagongshe.com/reaction/372966

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 in ethyl acetate, washed with 1% aqueous sodium hydroxide, dried (MgSO4) and concentrated in vacuo to give a yellow oil residue. Kugelrohr distillation 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 numberUS05162308
Source datasetuspto-grants-1992_11
ORD IDord-8c2408f5a9134323bad4f1bc4ebb5239
Source noteuspto-grants-1992_11