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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170948Generated: October 26, 2026

Potassium Hydroxide → HCID 11964486, compound

https://huagongshe.com/reaction/1170948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant6-Bromo-1,1,1-trifluorohexaneHCID 13845471—
ReactantHCID 68712477HCID 68712477—
SolventMethanolHCID 887—
ProductHCID 11964486HCID 11964486—

Reaction Conditions

Temperature70 °C

Reaction Steps

3-hydroxy-6-chloroacridone (594 mg) was stirred in 10 ml of methanol, and 5 ml of methanolic KOH (30 mg/ml) was added (1 equiv. base), whereupon complete dissolution occurred. 1-Bromo-5-trifluoromethylpentane (2.03 g, 3 equiv.) was added and the solution heated at 70° C. overnight, forming a fine solid precipitate; after cooling, 0.35 g of pale yellow powder was collected by filtration. When the filtrate is heated another 2 days, the same quantity of product may be isolated in addition. The crude product was crystallized from methanol. Analogous procedures can be applied for preparation of compounds with the O(CH2)3CF3, O(CH2)4CF3, O(CH2)7CF3, and O(CH2)10CF3— side chains and including aromatic ketone derivatives bearing O(CH2)C2F5 and O(CH2)C3F7 side chains.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829578B1
Source datasetuspto-grants-2010_11
ORD IDord-c1856e012c564a0e9005aaad1199317e
Source noteuspto-grants-2010_11