HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Methyl 3-carbamimidoylbenzoate acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl 3-(5-methyl-1,2,4-oxadiazol-3-YL)benzoate | HCID 53429639 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-carbamimidoylbenzoate acetate | HCID 66985510 | — |
Reaction Steps
150 ml of acetic acid, 150 ml of water and 50 g of water-moist Raney nickel are added to a solution of 327 g (1.47 mol) of methyl 3-(5-methyl-1,2,4-oxadiazol-3-yl)benzoate in 3 l of methanol, and the mixture is hydrogenated at room temperature and atmospheric pressure for 18 hours. The catalyst is filtered off, and the filtrate is evaporated. The residue is taken up in tert-butyl methyl ether, heated to the boil and filtered off with suction. The residue is dried in vacuo: 3-methoxycarbonylbenzamidinium acetate as colourless crystals; m.p. 222°; ESI 179 (M+H); HPLC: Rt.=1.40 min (method A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877751B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-4b207866bef24aa2bdebbf6b53031d8c |
| Source note | uspto-grants-2014_11 |