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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170947Generated: October 26, 2026

Ethanol → 3-(6,6,6-Trifluorohexyloxy)-6-hydroxyxanthone

https://huagongshe.com/reaction/1170947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant3,6-dihydroxy-9H-xanthen-9-oneHCID 5749322—
Reactant6-Bromo-1,1,1-trifluorohexaneHCID 13845471—
SolventWaterHCID 962—
Product3-(6,6,6-Trifluorohexyloxy)-6-hydroxyxanthoneHCID 68771264—

Reaction Steps

To 3,6-dihydroxy-xanthone (0.58 g, 1 equivalent) is added 10 ml of ethanol, then 117 mg of KOH 0.8 equivalents), followed by 0.58 g of CF3(CH2)5Br (1 equivalent); after two hours of boiling this mixture, the pH had dropped to the acidic range, and another 100 mg of KOH was added and heating continued overnight. The cooled mixture was diluted with water (50 ml) and extracted with ethyl acetate (3×50 ml), the combined extracts washed with 5 ml of water and brought to dryness. Separation of the 3-component mixture was achieved by chromatography (100 g of silica gel, column diameter 5 cm) with solvents of increasing polarity: Solvents used: ethyl acetate (A), hexane (isomeric mixture) (B), ethanol (C)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829578B1
Source datasetuspto-grants-2010_11
ORD IDord-632095f8161a4f4bb137138c227a7b63
Source noteuspto-grants-2010_11