HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535306Generated: October 30, 2026
Diethyl Ether → Stannane, (4-chlorophenyl)trimethyl-
https://huagongshe.com/reaction/535306
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | HCID 178478191 | HCID 178478191 | — |
| Product | Stannane, (4-chlorophenyl)trimethyl- | HCID 139674 | 97% |
Reaction Steps
To a 1M solution of trimethyltin chloride in THF (92 ml, 92 mmol) was slowly added a 1M solution of 4-chlorophenylmagnesium bromide in Et2O (92 ml, 92 mmol) over a 40 min period at −10° C. so that the temperature never exceed 0° C. After the addition, the cooling bath was removed and the resulting suspension was stirred at RT for 1 h. A saturated aqueous solution of NH4Cl (14 ml) was added followed by water until complete dissolution of the precipitate. The mixture was transferred into a separating funnel and extracted with Et2O (3×). The combined organic fractions were dried over Na2SO4, filtered and evaporated to dryness. The resulting crude material was purified by Combi-Flash Companion™ (Isco Inc.) column chromatography (SiO2; isocratic elution with cyclohexane) to yield the title compound (24.47 g, 89 mmol, 97%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859535B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-9ea1ad047e78491daff65ebf3aff10e4 |
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| Source note | uspto-grants-2014_10 |
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