HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → HCID 178452801, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1,1-Dibromo-3,3,3-trifluoroacetone | HCID 550523 | — |
| Reactant | HCID 86641684 | HCID 86641684 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178452801 | HCID 178452801 | 67% |
Reaction Steps
A solution of NaOAc (0.6 g, 7.4 mmol) in water (1.5 mL) was treated with 3,3-dibromo-1,1,1-trifluoro-propan-2-one (2.2 g, 8.3 mmol) and the resulting mixture was heated to reflux for 30 min. After cooling, the solution was added to [4-(6-formyl-pyridin-3-yloxy)-phenyl]-carbamicacid t-butyl ester (2.3 g, 7.4 mmol) in ammonium hydroxide (30%, 23 mL). The reaction mixture was stirred at RT for 5 h, concentrated in vacuo and purified via chromatography to give {4-[3-(4-trifluoromethyl-1H-imidazol-2-yl)-phenoxy]-phenyl}-carbamic acid t-butyl ester (2.1 g, 67% yield). MS (ESI) m/z: (M+H+) 421.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486951B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-68a2456efdd7495481edde455fe75749 |
| Source note | uspto-grants-2013_07 |