Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86601209 | HCID 86601209 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86601208 | HCID 86601208 | — |
Reaction Steps
Add sodium borohydride (1.70 g, 0.045 mol) to a solution of 1-(3,5-bis-trifluoromethylbenzyl)-5-phenyl-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester (5.0 g, 0.011 mol) in EtOH (70 mL). Heat to reflux and stir for 2 hours. Cool to room temperature. Add the reaction mixture to 0.5 N HCl (200 mL) and methylene chloride (200 mL). Separate layers and extract aqueous layer with methylene chloride (50 mL). Combine organic layers, dry (magnesium sulfate), filter and concentrate to give [1-(3,5-bis-trifluoromethyl-benzyl)-5-phenyl-1H-[1,2,3]triazol-4-yl]-methanol. Dissolve [1-(3,5-bis-trifluoromethyl-benzyl)-5-phenyl-1H-[1,2,3]triazol-4-yl]-methanol (3.90 g, 0.0097 mol) in DMSO (30 mL) and add N,N-diispropylethylamine (6.77 mL, 0.039 mol). To this solution add sulfur trioxide pyridine complex (3.09 g, 0.019 mol) in DMSO (30 mL). Stir for 2 hours. Add the reaction mixture to ethyl acetate (150 mL) and 0.5 N HCl (200 mL), and separate layers. Extract aqueous layer with ethyl acetate (50 mL). Combine organic layers and wash with saturated, aqueous sodium bicarbonate (100 mL) and 1.0 N HCl (100 mL). Dry organic layers (magnesium sulfate), filter and concentrate to give the title compound: 1H NMR (500 MHz, DMSO) δ 9.91 (s, 1H), 8.02 (s, 1H), 7.69 (s, 2H), 7.55-7.49 (m, 5 H), 5.86 (s, 2 H); Mass spectrum (m/e): 400 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07320994B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-1936449e049c4019816a3df6aedb27e1 |
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| Source note | uspto-grants-2008_01 |
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