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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1245434Erstellt: 27. Oktober 2026

Potassium Carbonate → Ethyl 2-{3'-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yloxy}benzoate

https://huagongshe.com/reaction/1245434

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktBenzoic acid, 2-fluoro-, ethyl esterHCID 67953—
EduktTert-butyl(4'-hydroxybiphenyl-3-ylmethyl)methylcarbamateHCID 69643261—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylacetamideHCID 31374—
ProduktEthyl 2-{3'-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yloxy}benzoateHCID 21911050104,9%

Reaktionsschritte

2.15 g (12.8 mmol) of ethyl 2-fluorobenzoate and 1.9 g (14 mmol) of potassium carbonate are successively added to a solution of 4 g (12.8 mmol) of tert-butyl(4′-hydroxybiphenyl-3-ylmethyl)methylcarbamate in 45 ml of dimethylacetamide. The reaction medium is refluxed for 48 hours, cooled, diluted with water and extracted with ethyl acetate. The organic phase is dried over sodium sulfate, filtered and concentrated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture. 3.1 g of ethyl 2-{3′-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yloxy}benzoate are obtained in the form of a colorless oil, in a yield of 53%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07125869B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-26c73ab41c454dd1858f0eff7961aaa0
Quellennotizuspto-grants-2006_10