HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 45122014, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 57019543 | HCID 57019543 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 45122014 | HCID 45122014 | 41% |
Reaction Steps
In a 1-L flask equipped with a reflux condenser and a Dean-Stark trap, 3.0 g of 2-hydroxy-5-hexenoic acid, 400 ml of toluene and 30 mg of p-toluenesulfonic acid were added and refluxed under a nitrogen atmosphere. Water accumulated in the trap was eliminated from time to time. The mixture was cooled after refluxing for 72 hours. It was washed twice with 10 ml of a saturated aqueous solution of sodium hydrogencarbonate, and an obtained crude product was vacuum distilled in the presence of zinc oxide to obtain 1.06 g of desired 3,6-di(3-butenyl)-1,4-dioxane-2,5-dione (yield 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07557176B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-afc0acd40ba24d82a3167300d63e9864 |
| Source note | uspto-grants-2009_07 |