HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,3-Propanediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | 9,10-Dioxo-9,10-dihydroanthracene-2-carbaldehyde | HCID 344310 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,3-Propanediol | HCID 10442 | — |
| Product | HCID 616802 | HCID 616802 | — |
Reaction Steps
A mixture of anthraquinone-2-aldehyde (12.0 g), 1,3-propanediol (10 ml), and p-toluenesulfonic acid (20 mg) in toluene (300 ml) was heated under reflux with a removal of water formed from the condensation of anthraquinone aldehyde and 1,3-propane diol for 4 hours. The mixture was then cooled to room temperature, filtered off with suction, washed with water and diethyl ether, and dried under vacuum to afford anthraquinone-2-propaneacetal (12.5 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06998487B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-80e256c5d38242e3bfcf7e6c21b708e2 |
| Source note | uspto-grants-2006_02 |