HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399865Generated: October 25, 2026
Guanidine Hydrochloride → 2-[3-Phenylbenzoyl]guanidine hydrochloride
https://huagongshe.com/reaction/399865
Participants
| Role | Name | HCID | Charge |
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| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methyl 3-phenylbenzoate | HCID 9855857 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[3-Phenylbenzoyl]guanidine hydrochloride | HCID 18945407 | 17.6% |
Reaction Steps
To a solution of guanidine hydrochloride (2.7 g) in methanol (12 ml) was added sodium methoxide (5.13 g, 28% in methanol) and the mixture was stirred for 15 minutes under nitrogen. To this mixture was added a solution of methyl 3-phenylbenzoate (1.20 g) in methanol (2 ml) and the mixture was stirred for 6 hours. The reaction mixture was poured into a mixture of ethyl acetate (100 ml) and water (50 ml). The organic layer was successively washed with 5N-sodium hydroxide aqueous solution and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on alumina (100 ml) and eluted with chloroform-methanol (10:1). The fractions containing the desired product were collected and evaporated in vacuo. The residue was crystallized from 4N-hydrogen chloride-ethyl acetate. The crystalline was recrystallized from ethanol to afford 2-[3-phenylbenzoyl]guanidine hydrochloride (274.0 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05824691 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-0e2f8d909e844621b2cc05d5ca6ce18e |
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| Source note | uspto-grants-1998_10 |
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