HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177498Generated: November 1, 2026
Tributylstannane → Tributyl(1-(4-fluorophenyl)vinyl)stannane
https://huagongshe.com/reaction/1177498
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4'-Fluoroacetophenone | HCID 9828 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tributyl(1-(4-fluorophenyl)vinyl)stannane | HCID 67111781 | — |
Reaction Steps
To a solution of diisopropylamine (1.39 mL, 10.1 mmol) in 20 mL THF at 0° C. was added butyllithium (4.02 mL, 10.0 mmol). After 10 min, tributylstannane (2.45 mL, 9.23 mmol) was added. After 10 min, the reaction mixture was cooled to −78° C. and a solution of 1-(4-fluorophenyl)ethanone (1.09 mL, 9.05 mmol) in 10 mL THF was added slowly by syringe in portions over 10 min. After 10 min, triethylamine (9.43 mL, 67.9 mmol) and methanesulfonyl chloride (2.80 mL, 36.2 mmol) was added and the bath allowed to expire overnight. The reaction mixture was treated with 50 mL hexanes and filtered, rinsing with hexanes. The filtrate was extracted with ACN, and the hexanes layer was dried over sodium sulfate, filtered, and concentrated. Purification with C-18 silica gel, eluting with DCM/ACN, gave tributyl(1-(4-fluorophenyl)vinyl)stannane as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842685B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-3066f3183c6646c8be70942bba9e771b |
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| Source note | uspto-grants-2010_11 |
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