HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253095Generated: October 30, 2026
Water → tributyl(3,4-dihydro-2H-pyran-6-yl)stannane
https://huagongshe.com/reaction/253095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tributyl(3,4-dihydro-2H-pyran-6-yl)stannane | HCID 4216837 | — |
Reaction Steps
A mixture of 3,4-dihydro-2H-pyran (500 mg, 5.94 mmol) in THF (10 mL) was brought to −78° C. followed by the addition of tert-butyllithium (12.2 mL, 20.8 mmol, 1.7 M in pentane). The resulting yellow solution was brought to 0° C. and stirred for 15 min. The reaction was then cooled to −78° C. and tributyltin chloride (4.8 mL, 17.8 mmol) was slowly added. The reaction was monitored by TLC. Upon completion by TLC, water was added (20 mL) to the reaction. The organic phase was separated, washed with water, dried over MgSO4, concentrated and chromatographed on silica gel using hexanes (500 ml hexanes and 0.5 mL triethylamine). The title compound was obtained as a colorless oil. MS m/z: 375(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872009B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-c6d842b340334fcaa433e72bc76e9b08 |
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| Source note | uspto-grants-2011_01 |
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