HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840528Generated: October 31, 2026
Benzyl mercaptan → (Benzylsulfanyl)(tributyl)stannane
https://huagongshe.com/reaction/1840528
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Undec-4-ene | HCID 136496 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | (Benzylsulfanyl)(tributyl)stannane | HCID 12514237 | 95% |
Reaction Steps
]undec-7-ene (DBU) is added dropwise at 20° C., under argon, to a solution of benzenemethanethiol (11.72 ml; 100.0 mmol) in anhydrous DMF (20.0 ml). After 0.5 hour at 20° C., the reaction mixture is cooled to 0° C. and tributyltin chloride is added dropwise. The mixture is allowed to warm to room temperature and stirring is continued for 5 hours. The reaction mixture is taken up in pentane (400 ml), washed with water (3×300 ml) and brine (100 ml), washed with sodium sulphate, filtered and then concentrated under reduced pressure. 39.0 g of tributyl[(phenylmethyl)thio]stannane are obtained in the form of a colourless oil, which is used without further purification in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06680329B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-7bbc2c1703044a6ba3458c2cbf9f1523 |
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| Source note | uspto-grants-2004_01 |
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