HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → 2-Chloro-N-(2-ethoxy-2-oxoethyl)ethanimidic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Glycine ethyl ester | HCID 12176 | — |
| Product | 2-Chloro-N-(2-ethoxy-2-oxoethyl)ethanimidic acid | HCID 179518 | — |
Reaction Steps
The ester prepared in step 1 is reacted with chloroacetylchloride at a temperature of from about -10° to +10° C. in a suitable solvent in the presence of a suitable base to produce chloroacetylglycine ethyl ester. Solvents useful in this reaction include water, dichloromethane, and dichloroethane. Suitable bases include sodium bicarbonate, sodium carbonate, potassium carbonate, and sodium hydroxide. If the aminoacid is used in the form of its hydrochloride, a two-fold excess of base must be used.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04385923 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-62832c8bd1324093982ac98d05c42903 |
| Source note | uspto-grants-1983_05 |