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HRID 129346Erstellt: 25. Oktober 2026

Tetrahydrofuran → Methyl 4-(1-trans-tridecenyl)pyrrole-2-carboxylate

https://huagongshe.com/reaction/129346

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktDodecyltriphenylphosphonium bromideHCID 84955—
Eduktmethyl 4-formyl-1H-pyrrole-2-carboxylateHCID 640310—
EduktButyllithiumHCID 178418339—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelHexaneHCID 8058—
ProduktMethyl 4-(1-trans-tridecenyl)pyrrole-2-carboxylateHCID 1502333314%

Reaktionsschritte

To a tetrahydrofuran suspension (200 ml) of 32 g (62.7 mmol) of dodecyltriphenylphosphonium bromide was added dropwise 40 ml of a ca. 15% solution of n-butyllithium in hexane under ice-cooling. After stirring the reaction mixture for 30 minutes, the temperature was dropped to -78° C. A tetrahydrofuran solution (100 ml) of 4.8 g (31.4 mmol) of methyl 4-formylpyrrole-2-carboxylate was then added dropwise. After stirring for 1 hour, 190 of ethanol was further added thereto dropwise. The reaction mixture was stirred for 1.5 hour at -78° C., and for another 12 hours while the temperature was gradually raised to room temperature. The resulting mixture was diluted with water, extracted with ethyl acetate, washed with aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After removing he solvent under reduced pressure, the residue was purified by subjecting it to column chromatography (eluent: ethyl acetate/hexane=1/10) and by recrystallizing twice from hexane to obtain 1.30 g (14 % yield) of methyl 4-(1-trans-tridecenyl)pyrrole-2-carboxylate, m.p. 65°-67° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE035096
Quelldatensatzuspto-grants-1995_11
ORD IDord-ecb63c61172b43d8b9cf15955b0ff9d3
Quellennotizuspto-grants-1995_11