HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941002Generated: October 31, 2026
Water → 1-Methyl-4-(trifluoromethyl)pyrrole-3-carbonitrile
https://huagongshe.com/reaction/1941002
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 1-methyl-4-(trifluoromethyl)-1H-pyrrole-3-carboxylic acid | HCID 11788779 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Methyl-4-(trifluoromethyl)pyrrole-3-carbonitrile | HCID 21459551 | — |
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° to 110° C./2 mm Hg yields the title product as a white solid, 0.95 g (54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05702681 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-b08dae794bab4aefa3ff9b6a46bb676c |
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| Source note | uspto-grants-1997_12 |
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