HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 1,4-dihydro-3H-2-benzopyran-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethylbenzene | HCID 7500 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 1,4-dihydro-3H-2-benzopyran-3-one | HCID 78092 | — |
Reaction Steps
After the reaction, recovery of isochromanones can be carried out by concentration of reaction mixture or extraction with an organic solvent such as ethyl acetate, toluene, xylene and ethylbenzene. When the reaction mixture is separated into two layers, i.e., a water layer and a product layer, depending on the target isochromanones, it is possible to separate and remove the water layer. In particular, when the product is 3-isochromanone, the product layer is liquid at 85° C. or higher, so that solubility in water is low and the target compound can be recovered by separation operation. Further, distillation and purification under reduced pressure can give rise to highly pure 3-isochromanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06372921B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-b0d7205cb70c43dd8996e0cdfe36e75e |
| Source note | uspto-grants-2002_04 |