HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine → N-diaminomethylene-2-methyl-4-bromo-5-methylsulphonylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Methyl 4-bromo-5-methanesulfonyl-2-methylbenzoate | HCID 10590825 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-diaminomethylene-2-methyl-4-bromo-5-methylsulphonylbenzamide | HCID 10830518 | — |
Reaction Steps
A solution of 1.8 g of methyl 2-methyl-4-bromo-5-methylsulphonylbenzoate [obtainable in accordance with Ex. 1] and 1.5 g of guanidine in 50 ml of methanol is boiled for five hours, and the solvent is subsequently removed. The residue is treated with water and the remaining crystalline crop is filtered off with suction and treated with dil. sodium hydroxide solution. The solid residue is filtered off and recrystallized from ethanol, and N-diaminomethylene-2-methyl-4-bromo-5-methylsulphonylbenzamide is obtained, m.p. 207°-208°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849796 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-f2e65e16a3b9461baa6d04fc1bf7ecd8 |
| Source note | uspto-grants-1998_12 |