HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 54267635, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 10888318 | HCID 10888318 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54267635 | HCID 54267635 | — |
Reaction Steps
The general method for the preparation of the starting enol esters is illustrated by the following example: 0.063M of 3,3,7-trimethyl-oct-6-ene-1-al were added under stirring to a mixture consisting of 0.06M of triethylamine, 0.126M of acetic anhydride and 1.1 g of potassium acetate pre-heated to 80°. The reactive mixture was refluxed for approximately 7 h. After cooling to room temperature, toluene and water were added and the two phases separated. 3,3,7-Trimethyl-1,6-octadienyl acetate was then obtained as a toluene solution and finally isolated by evaporation at reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04922027 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-d169eb32a8744f0b9eaf3e8218e59bdb |
| Source note | uspto-grants-1990_05 |