HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801491Generated: October 31, 2026
Benzenemethanamine, 3-chloro- → Benzenemethanamine, 3-chloro-
https://huagongshe.com/reaction/1801491
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenemethanamine, 3-chloro- | HCID 77802 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Pyrazole-1-carboxamidine monohydrochloride | HCID 2734672 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzenemethanamine, 3-chloro- | HCID 77802 | — |
| Product | Diisopropylethylamine | HCID 81531 | — |
| Product | Pyrazole-1-carboxamidine monohydrochloride | HCID 2734672 | — |
| Product | HCID 178512446 | HCID 178512446 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349827B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-ff9c4825d4fb4f8cbedc279331739ee1 |
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| Source note | uspto-grants-2013_01 |
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