HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → N,N-bis(trimethylsilyl)Methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N,N-bis(trimethylsilyl)Methanesulfonamide | HCID 12503736 | — |
Reaction Steps
A glass reactor equipped with a stirrer, nitrogen inlet, reflux condenser and addition funnel was purged with nitrogen and charged with 29.1 g (0.30 mol) of methanesulfonamide, MeSO2NH2, where Me represents the methyl radical, 84.9 ml (0.605 mol) of triethylamine and 240 ml of dry benzene. Trimethylchlorosilane (129.5 ml, 1.00 mol) was then added through the addition funnel over a period of 15 minutes to the stirred mixture, followed by heating at the boiling point for three hours. The mixture was then diluted with 200 ml of hexane and stirring was continued for 30 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05068379 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-abc4716cdac84c6f91c8dbce364af083 |
| Source note | uspto-grants-1991_11 |