Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178455184 | HCID 178455184 | — |
| Solvent | Methyl iodide | HCID 6328 | — |
| Product | HCID 10263146 | HCID 10263146 | — |
| Product | HCID 67757478 | HCID 67757478 | — |
| Product | HCID 67757768 | HCID 67757768 | — |
Reaction Steps
A solution of 3-tert-butyldimethylsiloxymethyl-1H-1,2,4-triazole (8.0 g) in N,N-dimethylformamide (20 ml) was added dropwise at 0° C. to a mixture of 60% sodium hydride in oil (1.5 g), methyl iodide (2.8 ml) and N,N-dimethylformamide (80 ml) for 10 minutes. The mixture was stirred for 10 minutes, to which was added water (300 ml), followed by extraction with ethyl acetate (100 ml×3 times). The organic layer was washed with a saturated aqueous sodium chloride solution, which was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The concentrate was subjected to a silica gel chromatography, eluting with ethyl acetate-hexane (1:1), then further with ethyl acetate. The object fractions were respectively concentrated under reduced pressure to afford 5-tert-butyldimethylsiloxymethyl-1-methyl-1H-1,2,4-triazole (4.4 g), 3-tert-butyldimethylsiloxymethyl-1-methyl-1H-1,2,4-triazole (2.4 g), and 3-tert-butyldimethylsiloxymethyl-4-methyl-4H-1,2,4-triazole (0.50 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05405861 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-72cb8adcd36d4abfa70504fcd43e4905 |
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| Source note | uspto-grants-1995_04 |
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