HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571437Generated: October 31, 2026
Tributyltin Chloride → TRIBUTYL(4-METHOXYPHENYL)STANNANE
https://huagongshe.com/reaction/571437
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | HCID 178491912 | HCID 178491912 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | TRIBUTYL(4-METHOXYPHENYL)STANNANE | HCID 2762547 | 80.2% |
Reaction Steps
To tributyltin chloride (652 mg, 2.00 mmol, 1.00 equiv) in THF (2 mL) at 23° C. was added 4-methoxyphenylmagnesium bromide (0.50 M in THF, 8.0 mL, 4.0 mmol, 2.0 equiv). After stirring for 1.0 hr at 60° C., the reaction mixture was cooled to 0° C. and quenched with saturated aqueous NH4Cl (10 mL), and Et2O (10 mL) was added. The phases were separated and the aqueous phase was extracted with Et2O (2×10 mL). The combined organic phases were washed with brine (10 mL) and dried (Na2SO4). The filtrate was concentrated in vacuo and the residue was purified by fractional distillation to afford 637 mg of the title compound as a colorless oil (80% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09024093B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-35f2ab8166e645d58d780cb2a677545c |
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| Source note | uspto-grants-2015_05 |
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