HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 1,1-Diethoxy-3-methyl-2-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | 3,7,11,15,19-Pentamethyl-2,6-eicosadienal | HCID 53817517 | — |
| Product | 1,1-Diethoxy-3-methyl-2-butene | HCID 5215320 | — |
Reaction Steps
0.1 Part of the reaction product, 1.74 parts of benzene, and 0.00018 part of benzoic acid were charged into a sealed tube, and reacted at 250°C. for 10 minutes. The product was subjected to gas chromatography analysis. It was thus confirmed that 3,7,11,15,19-pentamethyl-2,6-eicosadienal was obtained at the selectivity of 69.5% to the originally fed β-methyl-crotonaldehyde diethylacetal. The analytical value of the resulting acetal and aldehyde is shown in Table 16.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03978092 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-9608f64b06d74ba694ee1a5dc8811c3d |
| Source note | uspto-grants-1976_08 |