HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 2-Pentyl-4,4,7,7-tetramethyl-4,7-dihydro-1,3-dioxepin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Hexanal | HCID 6184 | — |
| Reactant | 2,5-Dimethyl-3-hexene-2,5-diol | HCID 349974 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Pentyl-4,4,7,7-tetramethyl-4,7-dihydro-1,3-dioxepin | HCID 21284700 | 70.3% |
Reaction Steps
A mixture of 720 g (5 moles) of 2,5-dimethylhex-3-ene-2,5-diol, 3 g of p-toluenesulfonic acid, 500 g (5 moles) of n-hexanal and 1 l of toluene was refluxed, and the resulting water of reaction (115 ml) was separated off in the course of 5.5 h. The mixture was then left to cool, 10 ml of a 25% strength aqueous sodium hydroxide solution were added, the mixture was washed neutral with a little water and the toluene was removed under reduced pressure at from 50° to 60° C. The residue obtained was distilled under 0.1 mbar to give 796 g of 2-pentyl-4,4,7,7-tetramethyl-4,7-dihydro-1,3-dioxepin of boiling point 75° C./0.1 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04761489 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-204a7f32307348a1bc31f43769c92109 |
| Source note | uspto-grants-1988_08 |