HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chromanone → Benzopyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chromanone | HCID 68110 | — |
| Reactant | Chroman-2-ol | HCID 11171070 | — |
| Product | Benzopyran | HCID 9211 | — |
Reaction Steps
In the same manner as described in Example 32, the formed chromanone compound was converted to a chromanol compound, and the dehydration reaction, separation and purification were carried out to obtain 6.58 g of a chromene compound represented by the following formula: ##STR167##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05106998 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-7936b4f234d142d2b3483e241537cd6b |
| Source note | uspto-grants-1992_04 |