HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39430Generated: October 23, 2026
Sodium Chlorite → 2-Cyclopropyl-4,6-bis-trifluoromethyl-benzoic acid
https://huagongshe.com/en/reaction/39430
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | 2-Cyclopropyl-4,6-bis-trifluoromethyl-benzaldehyde | HCID 58167762 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | 2-Methyl-2-butene | HCID 10553 | — |
| Product | 2-Cyclopropyl-4,6-bis-trifluoromethyl-benzoic acid | HCID 58167765 | — |
Reaction Steps
Crude 2-cyclopropyl-4,6-bis-trifluoromethyl-benzaldehyde (intermediate 0, 1.01 g, 3.58 mmol) was dissolved in 8.5 mL tert-butylalcohol and 4.5 mL 2-methyl-2-butene. At 0° C. a solution of sodium chlorite (340 mg, 3.76 mmol) and sodium dihydrogenphosphat (451 mg, 3.76 mmol) in 3 mL water was added. The reaction mixture was stirred at room temperature overnight. The solvents were evaporated off. The residue was taken up in 1N NaOH and extracted twice with tert-butyl methyl ether. The aqueous phase was adjusted to pH 2 by addition of 25% HCl and extracted twice with tert-butyl methyl ether. The combined organic phases were dried on sodium sulfate, filtered and evaporated. The crude material, off-white solid (1.01 g, 54%) was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524909B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-2e1ade2d28d9474d8de193c5da09005f |
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| Source note | uspto-grants-2013_09 |
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