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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437840Generated: November 1, 2026

HCID 11267833, compound → HCID 23134877, compound

https://huagongshe.com/reaction/1437840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11267833HCID 11267833—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 23134877HCID 23134877—

Reaction Steps

An ethanol solution (1.5 ml) of 3-chloro-5-(1-hydroxy-3,7-dimethyl-6-octenyl)-4,6-dihydroxy-2-methylbenzaldehyde (220) (196 mg, 0.57 mmol) was stirred at 0° C. in the presence of 5% Pd/C (50 mg) in a hydrogen atmosphere for 2 hours. After the catalyst was separated by filtration with the use of Celite, the filtrate was concentrated to obtain a crude product (188 mg). This crude product was purified by silica gel column chromatography (hexane:ethyl acetate=20:1) to obtain 3-chloro-5-(1-hydroxy-3,7-dimethyloctyl)-4,6-dihydroxy-2-methylbenzaldehyde (222, a diastereomeric mixture, red syrup 69 mg, crude yield 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622598B2
Source datasetuspto-grants-2009_11
ORD IDord-81ff34867deb4072b9e03638883fe2b5
Source noteuspto-grants-2009_11