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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 330174Erstellt: 25. Oktober 2026

Ethyl Acetate → methyl E-4-[5-[2-(t-butoxycarbonyl)-1-propenyl]-1-methylindol-3-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/330174

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Eduktt-Butyl (triphenylphosphoranylidene)propionateHCID 10916149—
EduktMethyl 4-(5-formyl-1-methylindol-3-ylmethyl)-3-methoxybenzoateHCID 14882555—
Lösungsmittel1,4-DioxaneHCID 31275—
Produktmethyl E-4-[5-[2-(t-butoxycarbonyl)-1-propenyl]-1-methylindol-3-ylmethyl]-3-methoxybenzoateHCID 1488255690%

Reaktionsschritte

A mixture of t-butyl (triphenylphosphoranylidene)propionate (10.41 g) and methyl 4-(5-formyl-1-methylindol-3-ylmethyl)-3-methoxybenzoate (4.5 g) in dry dioxane (60 ml) was stirred and heated at 100° for 18 hr, under an atmosphere of nitrogen. After ethyl acetate (100 ml) was added to the cooled reaction solution, solids were removed by filtration and the filtrate evaporated. The residual dark oil was purified by flash chromatography, eluting with 45:50:5 hexane: methylene chloride:ethyl acetate, to give methyl E-4-[5-[2-(t-butoxycarbonyl)-1-propenyl]-1-methylindol-3-ylmethyl]-3-methoxybenzoate (5.4 g, 90%) as a white foam: partial NMR (250 MHz, DMSO-6): 1.49 (s, 9H, t-butyl), 2.01(d, J=1.0 Hz, 3H, CCH3), 3.74(s, 3H), 3.82(s, 3H), 3.90(s, 3H), 4.05(s, 2H, ArCH2Ar').

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04894386
Quelldatensatzuspto-grants-1990_01
ORD IDord-218a44009ddd495586e58c9bb38047b0
Quellennotizuspto-grants-1990_01