HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170948Generated: October 26, 2026
Potassium Hydroxide → HCID 11964486, compound
https://huagongshe.com/reaction/1170948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Bromo-1,1,1-trifluorohexane | HCID 13845471 | — |
| Reactant | HCID 68712477 | HCID 68712477 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11964486 | HCID 11964486 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829578B1 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-c1856e012c564a0e9005aaad1199317e |
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| Source note | uspto-grants-2010_11 |
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