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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633917Generated: October 26, 2026

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

https://huagongshe.com/reaction/1633917

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 numberUS06503949B1
Source datasetuspto-grants-2003_01
ORD IDord-3d46ad9a739e4d60a06b417c1322a365
Source noteuspto-grants-2003_01