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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1669961Erstellt: 24. Oktober 2026

2,5-Dichloronitrobenzene → Escitalopram

https://huagongshe.com/de/reaction/1669961

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,5-DichloronitrobenzeneHCID 6977—
EduktOxalic acid dihydrateHCID 61373—
EduktCitadiol, (S)-HCID 7472057—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEscitalopramHCID 146570—
ProduktEscitalopram OxalateHCID 146571—

Reaktionsschritte

To a solution of 6 gm of (S)-(−)-4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxy-1-butyl]-3-(hydroxymethyl)benzonitrile in 60 ml tetrahydrofuran (THF) was added 4.33 gm of potassium tertiary butoxide at 0-10° C. and stirred for 30 minutes. A solution of 4.04 gm of 2,5-dichloronitrobenzene in 30 ml THF at 0-10° C. was added to it and stirred for 10-15 hours at room temperature, followed by addition of 250 ml of water. The reaction mixture was extracted with toluene, the toluene layer was washed with water and 5% sodium hydroxide solution and after acid base treatment yielded an oily product. The oil was dissolved in 16 ml of acetone at 30° C. and 1.75 gm of oxalic acid dihydrate in 8 ml acetone was added to it, stirred, cooled, filtered and dried at 60° C. to get the oxalic acid salt of (S)-(+)-1-[3-(dimethylamino) propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofuran carbonitrile.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07989645B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-6c65327698f545e2aa4c6b9ca64f2185
Quellennotizuspto-grants-2011_08