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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633916Generated: October 26, 2026

Potassium Carbonate → 4-[(4-Cyclopropylidenecyclohexylamino)methyl]benzoic acid methyl ester

https://huagongshe.com/reaction/1633916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-(aminomethyl)benzoate hydrochlorideHCID 2729253—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-CyclopropylidenecyclohexanoneHCID 22502174—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Solvent1,2-DichloropropaneHCID 6564—
Product4-[(4-Cyclopropylidenecyclohexylamino)methyl]benzoic acid methyl esterHCID 2355014035%

Reaction Steps

4-Aminomethylbenzoic acid methyl ester, hydrochloride salt (2.2 g, 11 mmol) was suspended in 1,2 dichloropropane (30 mL) and an aqueous saturated solution of potassium carbonate (15 mL) was added. The next day the organic phase was isolated and dried (MgSO4). 4-Cyclopropylidenecyclohexanone (1.5 g, 11 mmol) dissolved in dichloromethane (15 mL) was added followed by addition of acetic acid (400 μL) and sodium triacetoxyborohydride (3.3 g, 16.5 mmol). After 72 hours at 20° C. the reaction mixture was diluted with dichloromethane (50 mL) and 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 (50 g silica) using ethyl acetate and methanol (97:3) as eluent to give 1.1 g of 4-[(4-cyclopropylidenecyclohexylamino)methyl]benzoic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503949B1
Source datasetuspto-grants-2003_01
ORD IDord-845f7342b41040548f9c4870cf589567
Source noteuspto-grants-2003_01