HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 1-Trimethylsilyl-5-trimethylsilylthio-1,2,3-triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Saccharin | HCID 5143 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | HCID 178527741 | HCID 178527741 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Trimethylsilyl-5-trimethylsilylthio-1,2,3-triazole | HCID 20491074 | 96% |
Reaction Steps
1.52 ml of hexamethyldisilazane (7.3 mmoles) were added to a refluxing mixture of 0.49 (4.86 mmoles) of 5-mercapto-1,2,3-(1H)-triazole, 5 mg (0.207 mmole) of saccharin, 10 ml of ethyl acetate and 15 ml of dichloromethane and the ammonia evolved was titrated with 1 N H2SO4 by the method described in Example 1A. It was found that 2 equivalents (4.9 mmoles) were evolved after refluxing for 30 minutes. Volatile materials were evaporated in vacuo to obtain 1.19 g (96%) of 1-trimethylsilyl-5-trimethylsilylthio-1,2,3-triazole NMR Spectrum was taken in carbon tetrachloride solution: Δ0.31 (9H); 0.48 (9H); 7.46 (1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04400509 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-21c661c5a5a14e94a8fd2c81eb121e57 |
| Source note | uspto-grants-1983_08 |