HuagongsheHuagongshe Chemistry Print Report · For research reference only
Vinyl Acetate → HCID 86739833, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Vinyl Acetate | HCID 7904 | — |
| Reactant | HCID 86739834 | HCID 86739834 | — |
| Product | HCID 86739833 | HCID 86739833 | — |
Reaction Steps
Vinyl acetate and (1R,cis,E) 2,2-dimethyl-3-[2-fluoro-3-oxo-3-hydroxy-1-propenyl]-cyclopropane carboxylic acid were reacted in the presence of mercuric acetate as a catalyst to obtain (1R,cis,E) 2,2-dimethyl-3-[2-fluoro-3-oxo-3-ethenyloxy-1-propenyl]-cyclopropane carboxylic acid which was reacted with benzyl alcohol to obtain benzyl (1R,cis,E) 2,2-dimethyl-3-[2-fluoro-3-oxo-3-ethenyloxy-1-propenyl]-cyclopropanecarboxylate with a specific rotation of [α]D20 =+26° (c=1.2% in chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04489093 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-6dfdd4678cfc4123a9081ab5722bf46e |
| Source note | uspto-grants-1984_12 |