HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456296Generated: October 29, 2026
2-Methyl-2-butene → HCID 23089706, compound
https://huagongshe.com/reaction/456296
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | 4-(4-ethylphenoxy)benzaldehyde | HCID 10704429 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | Sodium Phosphate, Monobasic, Dihydrate | HCID 23673460 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 23089706 | HCID 23089706 | — |
Reaction Steps
An oxidation reaction (which is the method disclosed in Tetrahedron, (1987), 43, 4767-4776) was conducted using 4-(4-ethylphenoxy)benzaldehyde (which is the compound disclosed in J. Med. Chem., (1996), 39, 3984-3997, 500 mg, 2.21 mmol). 2-Methyl-2-butene (940 μL, 8.84 mmol), sodium dihydrogen phosphate dihydrate (338 mg, 2.16 mmol), and sodium chlorite (80%, 875 mg, 7.74 mmol) were added to a mixture solution of tert-butanol (3.6 mL) and water (1.0 mL) containing 4-(4-ethylphenoxy)benzaldehyde. The resulting mixture was stirred at room temperature, and the reaction was terminated with 1 N hydrochloric acid. After the extraction with ethyl acetate, the organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated to give 622 mg of 4-(4-ethylphenoxy)benzoic acid (white powder, yield: quantitative). Then, the same reaction as in Example 9 (9b) was conducted using all this 4-(4-ethylphenoxy)benzoic acid to give 437 mg of the title compound (pale red powder, yield: 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497397B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-456e0e6a77fd4005bd7466d7e3555fb6 |
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| Source note | uspto-grants-2013_07 |
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