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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methyl-2-buteneHCID 10553—
Edukt4-(4-Trifluoromethylphenyl)thiophene-2-carbaldehydeHCID 11736954—
EduktSodium ChloriteHCID 23668197—
EduktMonosodium phosphateHCID 23672064—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
Produkt4-[4-(Trifluoromethyl)phenyl]thiophene-2-carboxylic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091237B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-6f39bd3263d74268b672227e11e8ee23
Quellennotizuspto-grants-2006_08