Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(Trifluoromethoxy)benzaldehyde | HCID 605139 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-[(3-Bromophenyl)amino]-1,1,1-trifluoro2-propanol | HCID 23506102 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 18407223 | HCID 18407223 | 119.2% |
Reaction Steps
EX-633B) The 3-[(3-bromophenyl)amino]-1,1,1-trifluoro-2-propanol (1.14 g, 4 mmol) from EX-633A and 3-(trifluoromethoxy)benzaldehyde (0.78 g, 4.1 mmol) were dissolved in dichloroethane (18 mL). Acetic acid (0.253 mL, 4.2 mmol) and solid NaBH(OAc)3 (1.07 g, 5.05 mmol) were added. The mixture was stirred at room temperature for 3 h. then acidified with 1 N HCl solution. After neutralizing to pH 7.5 with 2.5 N sodium hydroxide, the mixture was extracted with methylene chloride. The organic layer was washed with brine and water, then dried over anhydrous MgSO4, and evaporated to give 1.12 g (62%) of the desired N-3-bromophenyl-[[[3-(trifluoromethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol product as a brown oil, which was greater than 80% pure by reverse phase HPLC analysis. HRMS calcd. for C17H14NO2F6Br 458.0190 [M+H]+, found: 458.0199.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476057B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-3240cc2589a7437295e0cf47d765f95a |
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| Source note | uspto-grants-2002_11 |
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