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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131625Erstellt: 26. Oktober 2026

Water → 2-(Cyclopropylamino)-5-methyl-3,4-thiophenedicarboxylic acid, 3-ethyl 4-methyl ester

https://huagongshe.com/reaction/131625

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
EduktCyclopropyl isothiocyanateHCID 92463—
EduktMethyl 3-bromo-2-oxobutanoateHCID 11183175—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(Cyclopropylamino)-5-methyl-3,4-thiophenedicarboxylic acid, 3-ethyl 4-methyl esterHCID 8660357461,5%

Reaktionsschritte

To a solution of (triphenylphosphoranylidene)-acetic acid ethyl ester (15 g) in anhydrous tetrahydrofuran (100 ml) was added isothiocyanato-cyclopropane (4.4 g) and the mixture was refluxed under a nitrogen atmosphere for 20 hr. After allowing to cool to ambient temperature the reaction mixture was cooled to −78° C. and then a solution of 3-bromo-2-oxo-butanoic acid methyl ester (8.7 g) in anhydrous tetrahydrofuran (10 ml) was added. The resulting mixture was allowed to warm to ambient temperature and then refluxed for 20 hr., then ambient temperature for 2 days. The reaction was poured into water and extracted with diethyl ether. The collected organic extract was dried over magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography over silica, eluting with i-hexane/ethyl acetate (95:5) then triturated with i-hexane/diethyl ether (8:2) to give the sub-title compound as a solid (7.5 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384951B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-a0516163ebdb43e2bcca83e1983a1e95
Quellennotizuspto-grants-2008_06