Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | HCID 14706457 | HCID 14706457 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18657625 | HCID 18657625 | — |
Reaction Steps
A mixture of toluene (80 ml), phenylacetylene (6.7 ml) and (2R,3R)-3-azido-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-2-butanol (2 g) was heated for 8 hours at 130° C. After cooling, toluene was distilled off under reduced pressure. The residue was purified by silica gel chromatography (silica gel 50 g, eluent: ethyl acetate) to give Compound 58 (0.85 g) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05371100 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-aa051b2400a949f78c7fb8748e56a2df |
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| Source note | uspto-grants-1994_12 |
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