HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butanal → HCID 20550298, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butanal | HCID 261 | — |
| Reactant | HCID 178419645 | HCID 178419645 | — |
| Product | HCID 20550298 | HCID 20550298 | — |
Reaction Steps
For example, according to the above-cited British patent, one starts from 10-(2-tetrahydropyranyloxy-)dec-1-ynyl magnesium bromide, which is reacted with butyraldehyde to obtain 14-(-2-tetrahydropyranyloxy-)-tetradec-5-yn-4-ol, which is then dehydrated to 2-(-tetradec-11-en-9-ynyloxy-)-tetrahydropyranyl(cis, trans mixture); the latter, after acetylation and reduction, provides a cis-cis and cis-trans mixture of 9,11-tetradecadienyl-acetate. To obtain the desired cis-trans compound, a difficult and expensive separation of the isomers is required.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04317905 |
| Source dataset | uspto-grants-1982_03 |
| ORD ID | ord-9b66a78c50cd4710a418e265feb3f4e6 |
| Source note | uspto-grants-1982_03 |