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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437842Generated: November 3, 2026

Ascofuranone → HCID 23134887, compound

https://huagongshe.com/reaction/1437842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAscofuranoneHCID 6434242—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 23134887HCID 23134887—

Reaction Steps

An ethanol (201 ml) solution of ascofuranone (1,058 mg, 2.52 mmlo) was stirred in the presence of 5% Pd/C (435 mg) in a hydrogen atmosphere at 0(C for three hours. After the catalyst was separated by filtration with the use of Celite, the filtrate was concentrated to obtain a crude product (1,178 mg). This product was purified by silica gel column chromatography (hexane:ethyl acetate═5:1) to obtain 3-chloro-4,6-dihydroxy-2-methyl-5-[3-methyl-7-(tetrahydro-5,5-dimethyl-4-oxo-2-furanyl)-octyl]benzaldehyde (a diastereomeric mixture, yellow syrup 262 mg, yield 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622598B2
Source datasetuspto-grants-2009_11
ORD IDord-5a6da47d821b44999f610e74ae848410
Source noteuspto-grants-2009_11