Ethylene → 1,9-Decadiene

HRID 596274Notes

Reaction equation

[CH:1]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1.[CH2:9]=[CH2:10]>>[CH2:9]=[CH:10][CH2:1][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH:3]=[CH2:2]

Participants

Reactant 2

HCID 6325Ethylene

HCID 136091-Cyclooctene

Product 1

HCID 154391,9-Decadiene

Procedure

A mixture of cyclooctene and ethylene was contacted with catalyst and adjuvant as in Examples IX and X at room temperature and 25 psi pressure to yield 13 weight percent 1,9-decadiene. This shows that ethylene and a cyclic olefin are converted to an acyclic polyene.

Workup

customwas contacted with catalyst and adjuvant as in Examples IX and X at room temperature

Sources & evidence

ORD record: ord-7aff1e554ec1439c828137a33e5a9a23
Source dataset: uspto-grants-1977_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04010217

Reaction notes

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