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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1633917Erstellt: 26. Oktober 2026

P-Toluenesulfonylhydrazide → 4-[(4-Cyclopropylcyclohexylamino)methyl]benzoic acid methyl ester

https://huagongshe.com/reaction/1633917

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktP-ToluenesulfonylhydrazideHCID 15303—
Edukt4-[(4-Cyclopropylidenecyclohexylamino)methyl]benzoic acid methyl esterHCID 23550140—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-[(4-Cyclopropylcyclohexylamino)methyl]benzoic acid methyl esterHCID 23550139—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

4-[(4-Cyclopropylidenecyclohexylamino)methyl]benzoic acid methyl ester (1.1 g, 3.9 mmol) was dissolved in DMF (40 mL) and p-toluenesulfonic acid hydrazide (2.8 g, 15.4 mmol) was added. The reaction was heated to 100° C. for 16 hours. After cooling to room temperature the reaction mixture was diluted with ethyl acetate (75 mL) and water (40 mL) was added. The aqueous phase was extracted with ethyl acetate (25 mL) and the combined organic phases washed with aqueous saturated sodium hydrogen carbonate (2×30 mL) and water (5×30 mL). The organic phase was dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography (25 g silica) using heptane and ethyl acetate (1:1) as eluent to give 4-[(4-cyclopropylcyclohexylamino)methyl]benzoic acid methyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06503949B1
Quelldatensatzuspto-grants-2003_01
ORD IDord-3d46ad9a739e4d60a06b417c1322a365
Quellennotizuspto-grants-2003_01