HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycine → HCID 178505159, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycine | HCID 750 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 56613771 | HCID 56613771 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178505159 | HCID 178505159 | 55% |
Reaction Steps
A mixture of 0.57 g (7.6 mol) of glycine, of 0.3 g (7.6 mmol) of sodium hydroxide in 3 cm3 of water and of 2.0 g (7.6 mmol) of N-(4-cyanophenyl)-N'-methylsulfonyl-S-methylisothiourea in 30 cm3 of 95% ethanol is heated at boiling point for 7 hours. After cooling, the precipitate obtained is filtered and dissolved in 20 cm3 of a 1N sodium hydroxide solution. The solution obtained is washed with dichloromethane (3×10 cm3) and ethyl acetate (2×10 cm3) then acidified to a pH close to 3 with a 6N HCl solution. After cooling, the precipitate obtained is filtered, washed with water (2×5 cm3) and dried in vacuo to give N-[methylsulfonylimino(4-cyanophenylamino)methyl]-2-aminoethanoic acid (yield 55%) having a melting point of 170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04921939 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-9f28cf1469da400794938187462bac62 |
| Source note | uspto-grants-1990_05 |