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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051635Generated: October 31, 2026

1,3-Butadiene → HCID 537535, compound

https://huagongshe.com/reaction/2051635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-ButadieneHCID 7845—
Reactant1,7-Octadien-3-olHCID 545738—
Reactant1,7-octadien-3-oneHCID 11804752—
SolventAcetic AcidHCID 176—
ProductHCID 537535HCID 537535—

Reaction Steps

1,7-Octadien-3-ol, Compound (III), which is the starting material for preparing 1,7-octadien-3-one of this invention can easily be synthesized by dimerizing butadiene using a palladium complex as a catalyst in the presence of acetic acid to obtain 3-acetoxy-1,7-octadiene, Compound (I), and then hydrolyzing the same. (See Tetrahedron Letters, No. 26, page 2451, 1967 incorporated herein by reference which teaches the synthesis of 4-acetoxy-2,7-octadiene and 1-acetoxy-2,7-octadiene by dimerizing butadiene in the presence of a bis(triphenyl phosphine) (maleic anhydride) palladium catalyst and acetic acid at 120° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04181683
Source datasetuspto-grants-1980_01
ORD IDord-5c251e8d37ec45118948c4b87c67d129
Source noteuspto-grants-1980_01