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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1777360Erstellt: 25. Oktober 2026

1-Hydroxybenzotriazole hydrate → (4-(5-(3-Chloro-4-isobutylphenyl)-1,2,4-oxadiazol-3-yl)phenyl)methanol

https://huagongshe.com/reaction/1777360

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
Edukt3-chloro-4-(2-methylpropyl)Benzoic acidHCID 59316720—
EduktHCID 178513316HCID 178513316—
LösungsmittelDimethylformamideHCID 6228—
Produkt(4-(5-(3-Chloro-4-isobutylphenyl)-1,2,4-oxadiazol-3-yl)phenyl)methanolHCID 70869326—

Reaktionsbedingungen

Temperatur122.5 °C

Reaktionsschritte

N,N-Dicyclohexylcarbodiimide (1.07 g, 0.0052 mol) is added to a solution of 3-chloro-4-isobutylbenzoic acid (0.74 g, 0.0035 mol), N-hydroxy-4-hydroxymethylbenzamidine (0.867 g, 0.0052 mol) and N-hydroxybenzotriazole monohydrate (0.798 g, 0.0052 mol) in N,N-dimethylformamide (15 mL). The reaction mixture is heated at 120-125° C. for 2 hrs. It is then cooled to 0-5° C., filtered and washed with dichloromethane (2×20 mL). The filtrate is evaporated under reduced pressure and the residue is treated with demineralized water (20 mL). It is extracted with ethyl acetate (2×30 mL) and the combined extract is dried over sodium sulfate. Removal of solvent under reduced pressure gives a crude residue which is purified by column chromatography (silica gel 230-400, ethyl acetate:toluene, 15:85) to give {4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-phenyl}methanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09266867B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-009c44ae601f4be8b37956c68656d75a
Quellennotizuspto-grants-2016_02