HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Benzenesulfonyl)-7-methoxy-2-benzofuran-1(3H)-one → HCID 20266223, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Benzenesulfonyl)-7-methoxy-2-benzofuran-1(3H)-one | HCID 10957672 | — |
| Reactant | HCID 13457043 | HCID 13457043 | — |
| Reactant | 2-Propanol, 2-methyl-, lithium salt (1:1) | HCID 23664764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20266223 | HCID 20266223 | 95% |
Reaction Steps
Continuing with a synthesis utilizing the object compound (5) to produce the tetrahydronaphthacene dione intermediate, the anion of 7-methoxy-3-phenylsulfonyl-1(3H)-isobenzofuranone (6) as generated at -78° C. using lithium t-butoxide in THF and reacted with the hexahydronaphthalenone (5) to furnish 9-acetyl-5,12-dihydroxy-4-methoxy-6(11H)-hexahydronaphthacenone (7) in 95% yield. Conversion of (7) to 9-acetyl-6-hydroxy-4-methoxy-7,8,9,10-tetrahydronaphthacene-5,12-dione (8) was achieved by heating (7) in dimethylforamide under oxygen at 45° C. for 18 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04543428 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-3d8905cbc3e1472e900f3df40e651b1e |
| Source note | uspto-grants-1985_09 |