HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596558Generated: October 30, 2026
Iodine → Triethyl(propyl)phosphanium iodide
https://huagongshe.com/reaction/596558
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Oxetane | HCID 10423 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Bromostyrene | HCID 16263 | — |
| Reactant | Triethylphosphine | HCID 27365 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | 1,2-Diethenylbenzene | HCID 66666 | — |
| Product | Triethyl(propyl)phosphanium iodide | HCID 21450067 | — |
Reaction Steps
The catalyst of this example was prepared from a cross-linked copolymer of a 2:1 molar ratio of styrene and p-bromo styrene and 2% by weight, based on the above monomers, of divinyl monomers. The latter in this instance was divinyl benzene. The Br of the polymer was replaced with Li and then the Li was converted to --(CH2)3OH by reaction with trimethylene oxide. The OH of the --(CH2)3OH was converted to the iodide with I2 in the presence of triphenyl phosphine. The cross-linked polymer having a plurality of --(CH2)3I groups was then reacted with triethyl phosphine to form the corresponding triethyl n-propyl phosphonium iodide. The iodide was converted to the acetate with sodium acetate and the acetate was converted to --OC2H5 /OH- by reaction with an 80-20 ethanol-water mixture (by volume) containing 3.7 g. Na in 200 ml. of the ethanol-water mixture. This catalyst had a plurality of ##STR3##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04011268 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-a0fe6795082a48479908dbd305cf99b2 |
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| Source note | uspto-grants-1977_03 |
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