HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374872Generated: October 30, 2026
Water → N-(4-Benzoyl-2-methylphenyl)-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide
https://huagongshe.com/reaction/374872
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Benzophenone, 4-amino-3-methyl- | HCID 21052 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3,3,3-Trifluoro-2-hydroxy-2-methylpropanoic acid | HCID 2775125 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Solvent | Ethyl ether methylene chloride | HCID 21881112 | — |
| Product | N-(4-Benzoyl-2-methylphenyl)-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide | HCID 9819831 | — |
Reaction Steps
To a solution of 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid (1.11 g) in N,N-dimethylacetamide (15 mL) at -20° C. was added thionyl chloride (0.84 g) and the mixture was allowed to stir at -10° to -15° C. for 1 hour. 4-Amino-3-methylbenzophenone (1.00 g) was added in one portion and the reaction mixture was stirred at room temperature overnight. The mixture was poured into water and the resultant gummy solid was collected by filtration. The solid was dissolved in methylene chloride, dried and evaporated to give a brown oil. Chromatography, with diethyl ether:dichloromethane (2:98) as the eluent, gave a white foam which was stirred with hexane for two hours. The title compound was collected by filtration as a white solid (1.04 g); mp 123°-124° C.; MS: m/z=352(M+1); NMR: 1.61 (s,3), 2.28 (s,3), 7.54-7.61 (m,3) 7.66-7.74 (m,6) 9.73 (s,1). Analysis for C18H16F3NO3 : Calculated: C, 61.54; H, 4.59; N, 3.99; Found: C, 61.53; H, 4.73; N, 4.01.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05482969 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-8a01073b36c24dc79dbb4f0545aeedcb |
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| Source note | uspto-grants-1996_01 |
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