HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(3-(4-Chlorobenzyl)-2,3,4,8-tetrahydrochromeno[6,7-e][1,3]oxazin-7-yl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Reactant | Phenoxodiol | HCID 219100 | — |
| Product | 4-(3-(4-Chlorobenzyl)-2,3,4,8-tetrahydrochromeno[6,7-e][1,3]oxazin-7-yl)phenol | HCID 25007599 | 88% |
Reaction Steps
4′,7-Dihydroxyisoflav-3-ene (506 mg, 2.11 mmol) was dissolved in ethanol (8 ml). 4-Chlorobenzylamine (0.33 ml, 2.70 mmol) was added followed by formaldehyde solution (2 ml, 0.03 mol, 37% wt.). The reaction was stirred at room temperature for 4 days. The white precipitate was collected to afford the title compound (748 mg, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367659B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-8846c1463c7c44188ba99fb43d9feeb2 |
| Source note | uspto-grants-2013_02 |