HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycine → N-Chloroacetylglycine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycine | HCID 750 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-Chloroacetylglycine | HCID 233485 | 84.5% |
Reaction Steps
Glycine (1.5 g, 20 mmol) was dissolved in 2N NaOH (25 ml, 50 mmol) and ether (20 ml) was added. Chloroacetyl chloride (2.26 g) dissolved in Et2O (20 ml) was added dropwise at 0° C. The mixture was stirred at 0° for 30 minutes and at room temperature 1 hour. The layers were separated and the water layer was washed with Et2O (2×20 ml). The water layer was then acidified to pH 2 with concentrated HCl and the product was extracted into EtOAc (3×50 ml). The combined EtOAc extracts were washed with brine, dried (MgSO4), and freed of solvent in vacuo to give title acid compound as a solid (2.56 g, 84%) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04734425 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-23aff94fff4f4992854c02a5465c4fe5 |
| Source note | uspto-grants-1988_03 |