HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9640Erstellt: 24. Oktober 2026
2-Methyl-2-butene → 4-[4-(Trifluoromethyl)phenyl]thiophene-2-carboxylic acid
https://huagongshe.com/de/reaction/9640
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Methyl-2-butene | HCID 10553 | — |
| Edukt | 4-(4-Trifluoromethylphenyl)thiophene-2-carbaldehyde | HCID 11736954 | — |
| Edukt | Sodium Chlorite | HCID 23668197 | — |
| Edukt | Monosodium phosphate | HCID 23672064 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | 4-[4-(Trifluoromethyl)phenyl]thiophene-2-carboxylic acid | HCID 21986512 | — |
Reaktionsschritte
A solution of 4-[4-(trifluoromethyl)phenyl]thiophene-2-carbaldehyde (intermediate 37, 1.23 g), t-butanol (20 ml) and 2-methyl-2-butene (10 ml) was cooled to 0° C. To this was added drop-wise, a solution of sodium chlorite (3.8 g) and sodium dihydrogen phosphate (4.03 g) in water (15 ml). After the addition was complete, the mixture was allowed to warm to room temperature and was stirred for 4 hours. The solution was then concentrated and partitioned between water and ethyl acetate. The aqueous layer was washed with a second ethyl acetate portion and the organic liquors were combined, washed with brine, then dried (MgSO4). The solution was then absorbed onto silica and loaded onto a SPE (Si) cartridge. The product was eluted with neat ethyl acetate to afford the title compound as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07091237B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-6f39bd3263d74268b672227e11e8ee23 |
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| Quellennotiz | uspto-grants-2006_08 |
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