HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyltin chloride → Stannane, trimethyl(3-methylphenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418370 | HCID 178418370 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Stannane, trimethyl(3-methylphenyl)- | HCID 617758 | — |
Reaction Steps
To a solution of 21.5 g (100 mmol) trimethyltin chloride in 500 mL THF at -35° C. was added 113 mL (113 mmol) 1.0M p-tolylmagnesium bromide over 3 minutes. The mixture was allowed to warm to RT and stir for 1 hour after which time was added saturated aqueous ammonium chloride. The mixture was extracted three times with ether. The combined organic material was washed with brine, was dried over MgSO4, was stripped of solvent in vacuo, then was distilled at 0.1 Torr with the title compound distilling between 66°-74° C. The bitolyl remaining in the still pot crystallized upon cooling. The title compound was isolated as a clear, shiny liquid, 25.4 (92% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250521 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-367d2e8bbb59487095482a6ec03273e7 |
| Source note | uspto-grants-1993_10 |