HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768672Generated: October 31, 2026
Pyridine → 4-(1,1-Difluoro-2,2-dimethylpropyl)benzoic acid
https://huagongshe.com/reaction/1768672
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 4-(1,1-Difluoro-2,2-dimethylpropyl) toluene | HCID 22261761 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(1,1-Difluoro-2,2-dimethylpropyl)benzoic acid | HCID 15232839 | — |
Reaction Steps
A mixture of 13.5 grams (68.1 mmoles) of 4-(1,1-difluoro-2,2-dimethylpropyl) toluene, 6.8 grams (170 mmoles) of sodium hydroxide and 21.5 grams (136 mmoles) of potassium permanganate in 250 ml. of 1:1 pyridine:water is heated to 95° C. and stirred for 4 hours. This suspension is filtered, and the residue is wash with 300 ml. of water and 400 ml. of ethyl acetate. The filtrate is concentrated in vacuo and then redissolved in 300 ml. of water. The aqueous solution is washed with 500 ml. of ethyl acetate and then acidified to pH2 with concentrated hydrochloric acid. This is extracted 3 times with 300 ml. of ethyl acetate, and the combined extracts are dried over magnesium sulfate and concentrated in vacuo to yield 4-(1,1-difluoro-2,2-dimethyl propyl)benzoic acid as a fine white powder. A portion of this material is recrystallized from diethyl ether to give colorless crystals of the acid (m.p. 196°-198° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05378728 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-5e5a4271677748578d6a76cc71c7de90 |
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| Source note | uspto-grants-1995_01 |
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