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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719983Generated: October 29, 2026

3-(Benzenesulfonyl)-7-methoxy-2-benzofuran-1(3H)-one → HCID 20266223, compound

https://huagongshe.com/reaction/1719983

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Benzenesulfonyl)-7-methoxy-2-benzofuran-1(3H)-oneHCID 10957672—
ReactantHCID 13457043HCID 13457043—
Reactant2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20266223HCID 2026622395%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04543428
Source datasetuspto-grants-1985_09
ORD IDord-3d8905cbc3e1472e900f3df40e651b1e
Source noteuspto-grants-1985_09