HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965819Generated: October 31, 2026
N-vinyl-2-pyrrolidone → HCID 22037088, compound
https://huagongshe.com/reaction/965819
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-vinyl-2-pyrrolidone | HCID 6917 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 3,5-di(trifluoromethyl)benzoate radical | HCID 141265 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22037088 | HCID 22037088 | — |
Reaction Steps
Trimethylsilyldiazomethane (11.5 mL) was added drop-wise to a solution of 3,5-bis-(trifluoromethyl)benzoic acid (2 g) in dry toluene (20 mL) and methanol (0.5 mL) previously cooled to 0° C. under a nitrogen atmosphere. The solution was stirred at r.t. for 1 hr, then concentrated in vacuo to give 3,5-bis-(trifluoromethyl)benzoic acid methyl ester (2 g) as a colourless oil. A solution of 3,5-bis-(trifluoromethyl)-benzoic acid methyl ester (2 g) and 1-vinyl-2-pyrrolidinone (863 μL) was added to a mixture of sodium hydride (60% suspension in mineral oil—0.41 g) in dry toluene (30 mL) previously heated to reflux. The mixture was stirred for 12 hrs, then it was partitioned between saturated ammonium chloride solution and AcOEt. The organic layer was dried, concentrated in vacuo and the residue was purified by flash chromatography (CH/AcOEt 8:2) to give the title compound (1.6 g) as a beige oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06951861B1 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-8cd443e7093a43c08b8aeee271c86cd3 |
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| Source note | uspto-grants-2005_10 |
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