Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Triphenyltin Chloride | HCID 12540 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | Triphenylstannane | HCID 6460 | 100% |
Reaction Steps
3.9 g of sodium borohydride (0.1 mol) and 70 ml of monoglyme were mixed together in a 200 ml eggplant type flask and cooled to -10° C. 70 ml of a diglyme solution containing 10.0 g of triphenyltin chloride (0.026 mol) was added to this mixture dropwise for 30 minutes. Subsequently, the mixture was stirred for another 30 minutes at -10° C. Then diglyme was removed under a reduced pressure of greater than 1 mmHg at below 0° C. Then, the resultant residue was extracted with diethylether followed by concentration under reduced pressure to yield 9.1 g of the final product of triphenyltin hydride (yield=100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06022822 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-c7b4f3644fb94eda8ba0b0c4d70f7677 |
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| Source note | uspto-grants-2000_02 |
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