HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54259Generated: October 28, 2026
Water → 3-(4-Fluorophenyl)-3-methyl-1-tributylstannyl-1-butene
https://huagongshe.com/reaction/54259
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3-(4-Fluorophenyl)-3-methyl-1-iodo-1-tributylstannylbutane | HCID 21467967 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Fluorophenyl)-3-methyl-1-tributylstannyl-1-butene | HCID 67631524 | 88.2% |
Reaction Steps
Under a nitrogen atmosphere, a stirred solution of 17.2 grams (0.030 mole ) of 3-(4-fluorophenyl)-3-methyl-1-iodo-1-tributylstannylbutane and 13.7 grams (0.090 mole) of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in 100 mL of tetrahydrofuran is heated at reflux for about 18 hours. The reaction mixture is cooled and poured into about 500 mL of water. The mixture is then made acidic with aqueous 2N hydrochloric acid and extracted with three 200 mL portions of diethyl ether. The combined extracts are dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residue. The residue is subjected to column chromatography on silica gel, using 5% methylene chloride in petroleum ether as the eluant. The product-containing fractions are combined and concentrated under reduced pressure, yielding 12.0 grams of 3-(4-fluorophenyl)-3-methyl-1-tributylstannyl-1-butene. The NMR spectrum is consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05622954 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-8160a919727843de88cd84d6a77a8bce |
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| Source note | uspto-grants-1997_04 |
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