HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261401Generated: October 26, 2026
4-Oxo-1-iodo-trans-1-octene → 4-Hydroxy-4-vinyl-1-iodo-trans-1-octene
https://huagongshe.com/reaction/261401
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Oxo-1-iodo-trans-1-octene | HCID 12851280 | — |
| Reactant | HCID 178461836 | HCID 178461836 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Hydroxy-4-vinyl-1-iodo-trans-1-octene | HCID 12851281 | — |
Reaction Steps
To a stirred solution of 7.8 ml of vinyl magnesium chloride (2.3M in tetrahydrofuran), at -25° C. is added a solution of 3.55 g of 4-oxo-1-iodo-trans-1-octene in 20 ml of tetrahydrofuran during 15 minutes. After the addition, the solution is stirred at -20° C. to -15° C. for 30 minutes. The reaction is quenched with a mixture of hexane and ice. The aqueous phase is separated and extracted with additional hexane. The combined hexane extracts are washed successively with water and brine. The solution is dried over magnesium sulfate and concentrated. The residue is subjected to dry column chromatography on silica gel with benzene as developing solvent to give a liquid, pmr spectrum (CDCl3): 5.2 (m, terminal CH2), 5.83 (q, CH=CH2), 6.13 (d, ICH=), and 6.52 (m, ICM=CH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04165331 |
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| Source dataset | uspto-grants-1979_08 |
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| ORD ID | ord-7dad8c3d0b1240aba3609505b6722021 |
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| Source note | uspto-grants-1979_08 |
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