HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 7-Isopropoxy-5-methyl-4-heptenal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23263480 | HCID 23263480 | — |
| Catalyst | Mercurous acetate | HCID 61181 | — |
| Solvent | Ethyl vinyl ether | HCID 8023 | — |
| Product | 7-Isopropoxy-5-methyl-4-heptenal | HCID 54043294 | — |
Reaction Steps
15.8 g (0.1 mol) of 5-isopropoxy-3-methyl-1-penten-3-ol (produced in accordance with Example 63) and 20.0 g of mercury acetate are kept in 180 cc of ethylvinyl ether at reflux temperature during the course of 4 days. 0.9 cc of glacial acetic acid is added at 20° to the solution which has rendered turbid. 150 cc of 5% potassium carbonate solution are added after 3 hours and the mixture is extracted with hexane. The hexane extract is evaporated and the residue is heated to 165°-168° during 11/2 hours in an atmosphere of nitrogen and without further purification; the residue is subsequently distilled at reduced pressure. B.P. of 7-isopropoxy-5-methyl-4-heptenal: 70°-73°/0.8 mm. nD20 = 1.4476
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03933804 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-a206865dee51418780f0e875f44cd156 |
| Source note | uspto-grants-1976_01 |