HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(Ethoxycarbonyl)alanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | L-Alanine | HCID 5950 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(Ethoxycarbonyl)alanine | HCID 10558934 | 96% |
Reaction Steps
Production of 3-(methyl ONN azoxy)-2,2-propylene dioxy-butane [Compound (IV):R3 =H, R4 =-CH2CH2CH2 -]: (a) In 700 ml of water were dissolved 40 g of L-alanine and 127 g of sodium carbonate. Then 64 ml of ethyl chloroformate was added dropwise to the mixture under ice-cooling and its stirring was conducted at room temperature for 30 minutes. A 35% hydrochloric acid was added to the reaction liquid to make this acidic and the reaction liquid was adsorbed on the column (6.5×60 cm) of diaion HP-20. After washing with water this was eluted with 70% methanol. The eluate was condensed under vacuum thereby to obtain 69 g (yield of 96%) of N-ethoxycarbonyl alanine as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05264559 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-95fe1a3e930745e0ac73978f46fa9e67 |
| Source note | uspto-grants-1993_11 |