HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 178448153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2-propylpropane-1,3-diol | HCID 7021156 | — |
| Reactant | 3-(3,5-Dichlorophenyl)propanal | HCID 18332054 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178448153 | HCID 178448153 | 72.1% |
Reaction Steps
A solution comprising 18.3 g (155.1 mmol) of 2-propyl-1,3-propanediol, 30.0 g (147.7 mmol) of 3-(3,5-dichlorophenyl)-propionaldehyde, 1.5 g of p-toluenesulfonic acid, and 300 ml of toluene was heated to reflux while taking out the distilled water for 3 hours. After termination of the reaction, the organic layer was washed with a diluted aqueous sodium bicarbonate solution once and water thrice, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under a reduced pressure and the residue was subjected to silica gel column chromatography (eluent: toluene) to obtain 32.3 g of a crude trans-2-(2-(3,5-dichlorophenyl)ethyl)-5-propyl-1,3-dioxane. (Yield: 72.1%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329027B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-42b8e955bf384898ac8a85db0a575b6c |
| Source note | uspto-grants-2001_12 |