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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801491Generated: October 31, 2026

Benzenemethanamine, 3-chloro- → Benzenemethanamine, 3-chloro-

https://huagongshe.com/reaction/1801491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenemethanamine, 3-chloro-HCID 77802—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyrazole-1-carboxamidine monohydrochlorideHCID 2734672—
SolventDimethylformamideHCID 6228—
ProductBenzenemethanamine, 3-chloro-HCID 77802—
ProductDiisopropylethylamineHCID 81531—
ProductPyrazole-1-carboxamidine monohydrochlorideHCID 2734672—
ProductHCID 178512446HCID 178512446—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 1 M solution of Hunig's Base in anhydrous DMF is prepared (Solution A). A 0.5 M solution of 1-H-pyrazole-1-carboxamidine hydrochloride is prepared using solution A. A 0.25 M solution of (3-chlorophenyl)methanamine in anhydrous DMF is prepared. A solution of (3-chlorophenyl)methanamine (800 μL, 200 mmol, 1.0 eq) is added to a solution of 1-H-pyrazole-1-carboxamidine hydrochloride (400 μL, 200 mmol, 1.0 eq) followed by addition of Hunig's Base (80 μL, 2.3 eq). The reaction mixture is heated at 100° C. for 24 hours. The solvent is removed under reduced pressure to give the crude desired product as a viscous oil. The crude product is dried by azeotoping with acetone and drying the residue under high vacuum. The crude 1-(3-chlorobenzyl)guanidinium chloride is used in the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349827B2
Source datasetuspto-grants-2013_01
ORD IDord-ff9c4825d4fb4f8cbedc279331739ee1
Source noteuspto-grants-2013_01