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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1678599Erstellt: 26. Oktober 2026

Tributylphosphine → Ethyl 3-(4-{[2-(benzyloxy)benzyl]oxy}-3,5-difluorophenyl)propanoate

https://huagongshe.com/reaction/1678599

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylphosphineHCID 13831—
Edukt1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Edukt2-(Benzyloxy)benzaldehydeHCID 344784—
EduktSodium borohydrideHCID 4311764—
EduktEthyl 3-(3,5-difluoro-4-hydroxyphenyl)propanoateHCID 23136305—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktEthyl 3-(4-{[2-(benzyloxy)benzyl]oxy}-3,5-difluorophenyl)propanoateHCID 2313628744,2%

Reaktionsschritte

2-(Benzyloxy)benzaldehyde (274 mg, 1.3 mmol) dissolved in methanol (20 mL), sodium borohydride (73 mg, 1.9 mmol) was added thereto, and then the mixture was stirred with ice cooling for 2 hours. To the reaction solution was added water, and the reaction mixture was extracted with ethyl acetate. The extract was dried, and then concentrated under reduced pressure. The residue was dissolved in tetrahydrofuran (10 mL). Ethyl 3-(3,5-difluoro-4-hydroxyphenyl)propanoate (200 mg, 0.86 mmol), tributylphosphine (0.23 mL, 1.1 mmol) and azodicarbonyldipiperidine (282 mg, 1.1 mmol) were added thereto, and the mixture was stirred at room temperature for 12 hours. The reaction solution was purified with alumina column chromatography (ethyl acetate) and silica gel column chromatography (hexane/ethyl acetate=100:0 to 80:20) to give the title compound (162 mg, yield 29%) as an oily matter.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08008525B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-548ce631baac49c4bd2df2324448bc0a
Quellennotizuspto-grants-2011_08