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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 459119Erstellt: 25. Oktober 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (1R,3S)-(2S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid 3-(biphenyl-4-yloxy)-1-cyclohexyl ester

https://huagongshe.com/reaction/459119

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Eduktalpha-Methoxy-alpha-trifluoromethylphenylacetic acid, (-)-HCID 6992788—
Edukt(1r*,3s*)-3-(Biphenyl-4-yloxy)-cyclohexanolHCID 58822848—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt(1R,3S)-(2S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid 3-(biphenyl-4-yloxy)-1-cyclohexyl esterHCID 58822646—

Reaktionsbedingungen

Temperatur36 °C

Reaktionsschritte

A mixture of (1R*,3S*)-3-(Biphenyl-4-yloxy)-cyclohexanol from Step C (1 eq) with (S)-(−)-α-methoxy-α-(trifluoromethyl)-phenylacetic acid (1 eq), DMAP (0.1 eq) and EDCI (1.2 eq) in dichloromethane was stirred at 36° C. over night. The reaction mixture was cooled and concentrated to dryness. Reconstituted in: ether and washed with HCl 1N, and NaHCO3. Dry over MsSO4 and concentrated in vacuo to give a crude that was purified by silica gel chromatography to give a diastereomeric mixture which was separated using chiral HPLC

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07192982B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-d431c381472f4e39838a945511b6736b
Quellennotizuspto-grants-2007_03