Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 178491706 | HCID 178491706 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10243171 | HCID 10243171 | 49% |
| Product | HCID 10444086 | HCID 10444086 | 34% |
Reaction Steps
To a solution of 3-p-methoxybenzylthio-1,2,4-triazole (10.0 g: 45.2 mMol.) in methanol (100 ml) is added under ice cooling a solution of diazomethane in ether (prepared from 15 g of N-nitrosomethylurea), and the mixture is stirred for 1 hour. The reaction mixture is concentrated and purified by Lobar column chromatography (toluene: ethyl acetate=1:2 to 1:3) to give 3-p-methoxybenzylthio-2-methyl-1,2,4-triazole [5.17 g: NMR δ(CDCl3) ppm: 3.63(s, 3H), 3.79(s, 3H), 4.34(s, 2H), 6.80-6.84, 7.19-7.24(A2B2, 4H), 7.88(s, 1H). IR ν(CHCl3) cm-1 : 1611, 1511, 1476, 1464, 1440, 1360, 1302. Yield: 49%] and 3-p-methoxybenzylthio-1-methyl-1,2,4-triazole [3.60 g: NMR δ(CDCl3) ppm: 3.78(s, 3H), 3.87(s, 3H), 4.31(s, 2H), 6.80-6.85, 7.30-7.34(A2B2, 4H), 7.99(s, 1H). IR ν(CHCl3) cm-1 : 1612, 1512, 1465, 1440, 1421, 1356, 1302. Yield: 34%].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05352792 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-5ebe5a29e3e546bdbc1df55fcc852d9c |
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| Source note | uspto-grants-1994_10 |
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