HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-Hydroxy-N-[(3-trifluoromethylphenyl)methyl]benzo[b]thiophene-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzoic acid, 2-mercapto-, methyl ester | HCID 21009 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-Chloro-N-(3-trifluoromethyl-benzyl)-acetamide | HCID 21277832 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Hydroxy-N-[(3-trifluoromethylphenyl)methyl]benzo[b]thiophene-2-carboxamide | HCID 54693826 | 78% |
Reaction Steps
To a solution of methyl thiosalicylate (0.67 g; 0.004M) in 20 ml of methanol is added solid sodium methoxide (0.65 g; 0.012M; 3 eqv.) followed by N-[(3-trifluoromethylphenyl)methyl]-chloroacetamide (1.0 g; 0.004M) and the mixture is refluxed under a nitrogen atmosphere for 30 minutes. The mixture is cooled to room temperature and added to a solution of 1.5 ml of glacial acetic acid in 25 ml of water and cooled to 0° C. The cream colored solid is collected, washed with 50% methanol-water, air dried, and recrystallized from nitromethane to give 1.05 g (78% yield) of the title compound; m.p. 139°-141° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04800211 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-77272ecc81fe45968481f3cc40a5a03e |
| Source note | uspto-grants-1989_01 |