HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Butadiene → HCID 537535, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | 1,7-Octadien-3-ol | HCID 545738 | — |
| Reactant | 1,7-octadien-3-one | HCID 11804752 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 537535 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04181683 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-5c251e8d37ec45118948c4b87c67d129 |
| Source note | uspto-grants-1980_01 |