HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 69316002, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | 2-Methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenal | HCID 102375 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69316002 | HCID 69316002 | — |
Reaction Steps
103 g (0.5 mol) of 2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenal, 38 g (0.5 mol) of 1,3-propanediol and 1 g of p-toluenesulfonic acid are heated with 200 g of toluene for 2.5 hours in a water separator. After cooling, the mixture is washed with soda solution and dried over sodium sulfate. 3 g of sodium carbonate are added and the mixture is distilled on a 30 cm packed column. At 122-126° C./1.6-0.82 mbar this yields 81 g of product comprising 66% of 2-[1-methyl-3-(2,6,6-trimethyl-1-cyclohexen-1-yl)allyl]-1,3-dioxane and also containing other isomers with double bonds.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07354893B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-be479ee4a43e4ee28bb5e1154716ed1a |
| Source note | uspto-grants-2008_04 |