Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814644Generated: October 25, 2026

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

https://huagongshe.com/reaction/1814644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ToluenesulfonylhydrazideHCID 15303—
Reactant4-[(4-Cyclopropylidenecyclohexylamino)methyl]benzoic acid methyl esterHCID 23550140—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-[(4-Cyclopropylcyclohexylamino)methyl]benzoic acid methyl esterHCID 23550139—

Reaction Conditions

Temperature100 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875760B2
Source datasetuspto-grants-2005_04
ORD IDord-40393486346a49a3a3ed325525e36609
Source noteuspto-grants-2005_04