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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330566Generated: October 31, 2026

HCID 13910822, compound → HCID 13910825, compound

https://huagongshe.com/reaction/330566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13910822HCID 13910822—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventHCID 178418361HCID 178418361—
ProductHCID 13910825HCID 1391082590.3%

Reaction Steps

2 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxy-carbonyl)-4-hydroxy-6-methoxy-7-benzyloxynaphthalene obtained in Example 6 are dissolved in a mixture of 200 ml of tetrahydrofuran and 50 ml of methanol. The solution is stirred in the presence of 2 g of 10% palladium-charcoal in hydrogen atomsphere at 40 psi for 2 hours. After the reaction, the catalyst is removed by filtration, and the filtrate is evaporated to dryness under reduced pressure. The resultant crude crystals are triturated with methanol, whereby 1.5 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)4-hydroxy-6-methoxy-7-hydroxynaphthalene is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04897418
Source datasetuspto-grants-1990_01
ORD IDord-edce34b5a6b14512864b56be438156d1
Source noteuspto-grants-1990_01