HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524982Generated: October 25, 2026
Sodium Hydroxide → N-o-Tolyl-3-(trifluoromethyl)-1H-pyrrole-2-carboxamide
https://huagongshe.com/reaction/524982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(Phenylsulfonyl)-N-o-tolyl-3-(trifluoromethyl)-1H-pyrrole-2-carboxamide | HCID 70922319 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-o-Tolyl-3-(trifluoromethyl)-1H-pyrrole-2-carboxamide | HCID 70922391 | 50% |
Reaction Steps
To a solution of 1-(phenylsulfonyl)-N-o-tolyl-3-(trifluoromethyl)-1H-pyrrole-2-carboxamide (560 mg of crude material) in 12 mL of methanol was added 2 mL of an aqueous 1N solution of sodium hydroxide and the mixture was stirred at room temperature during 1 h. At the end of this period, no starting material was detected and the reaction was elaborated in the following way: methanol was evaporated and water was added basifying the mixture with saturated aqueous solution of potassium carbonate. This mixture was extracted with ethyl acetate and this organic phase was washed with water and brine, dried (Na2SO4) and concentrated to dryness affording a reddish residue. This residue was purified by flash chromatography silica (hexane/ethyl ether). Concentration of the fractions containing the compound afforded 120 mg (50%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340547B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e065a7509ca44cf4b2e62554317bdcbc |
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| Source note | uspto-grants-2016_05 |
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