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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030690Generated: October 25, 2026

2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenone → 2'-Hydroxy-3'-isopentyl-4',6'-bis(methoxymethoxy)acetophenone

https://huagongshe.com/reaction/1030690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl2-butenyl)acetophenoneHCID 11099372—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
Product2'-Hydroxy-3'-isopentyl-4',6'-bis(methoxymethoxy)acetophenoneHCID 1609453182.8%

Reaction Steps

A solution of 2.08 g of the 2'-hydroxy-4',6'-bis(methoxymethoxy)-3'-(3-methyl-2-butenyl)acetophenone obtained in Production Example 13 in ethanol (20 ml) was added to a sufficiently hydrogen gas-absorbed suspension of 1.0 g of 5% palladium-carbon in 30 ml of ethanol, and the mixture was stirred at room temperature under atmospheric pressure in a hydrogen atmosphere. After the reaction, the reaction mixture was filtered, and the solvent was removed from the filtrate by distillation. The obtained residue was subjected to the silica gel column chromatography (3.0 cm in diameter, 60 g of silica gel, 0.3 kg/cm2) using a mixed solvent of n-hexane and ethyl acetate (n-hexane/ethyl acetate-3/1). Fractions of 50 ml were recovered, and 1.73 g (yield=82.8%) of 2'-hydroxy-3'-isopentyl-4',6'-bis(methoxymethoxy)acetophenone in the form of a yellow oil was obtained from the third to fifth fractions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106871
Source datasetuspto-grants-1992_04
ORD IDord-947296a762f14e6da0e7590ae1fa0b2e
Source noteuspto-grants-1992_04