HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → N-(4'-Amino-6-methylbiphenyl-3-yl)-3-(trifluoromethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | N-(6-Methyl-4'-nitrobiphenyl-3-yl)-3-(trifluoromethyl)benzamide | HCID 69273794 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4'-Amino-6-methylbiphenyl-3-yl)-3-(trifluoromethyl)benzamide | HCID 69046998 | 44.8% |
Reaction Steps
To N-(6-methyl-4′-nitrobiphenyl-3-yl)-3-(trifluoromethyl)benzamide (375 mg, 0.937 mmol) was added 1,4-dioxane (12 mL) and water (6.2 mL), then ammonium hydroxide (220 μL, 5.6 mmol) followed by sodium dithionite (1.4 g, 7.9 mmol). The reaction was stirred at ambient temperature until LCMS indicated complete reduction, typically 30-60 minutes. The reaction is accompanied by a color change from yellow to colorless. The reaction was partitioned between water and EtOAc and the organic phase was washed with water and saturated aqueous NaCl, then dried (MgSO4) and evaporated to leave the crude product (155 mg, 44.8%) which was used without further purification in the subsequent reaction. MS (EI) m/z=371 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513270B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-67786159925e4ff1bfdf53f62f5b753a |
| Source note | uspto-grants-2013_08 |