Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3,3,3-Trifluoro-2-hydroxy-2-methylpropanoic acid | HCID 2775125 | — |
| Reactant | HCID 10753680 | HCID 10753680 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 10692234 | HCID 10692234 | 72% |
Reaction Steps
To a stirred, cooled (-20° C.) solution of 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid (0.82 g, 5.2 mmol) in N,N-dimethylacetamide (10 mL) was added thionyl chloride (0.62 g, 5.2 mmol) and the mixture stirred at -10° to -15° C. for 1 hour. 4[(2-Cyanophenyl)sulphonyl]benzeneamine (1.00 g, 3.8 mmol) was added in one portion and the reaction mixture stirred at room temperature overnight. The mixture was poured-into water and the aqueous solution decanted from an oily solid which was purified by flash column chromatography (5% v/v ethyl acetate/methylene chloride). Recrystallization from methylene chloride/hexane yielded the title propanamide as a white solid (1.08 g, 72%); mp 156°-158° C. 1H--NMR (250 MHz, d6 --DMSO): 1.58 (s, 3H, CH3) 7.59 (s, 1H, OH) 7.88-8.13 (m, 7H, aromatic) 8.31 (d, 1H, J=6.9 Hz, aromatic) 10.50 (s, 1H, OH). MS (CI, CH4): 399 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05272163 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-6650fa204ea341e485a3ac6c12f34954 |
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| Source note | uspto-grants-1993_12 |
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