HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-acetoacetyl-L-aspartyl-L-phenylalanine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | L-Phenylalanine, methyl ester | HCID 736234 | — |
| Reactant | N-acetoacetyl-L-aspartic anhydride | HCID 13334674 | — |
| Product | N-acetoacetyl-L-aspartyl-L-phenylalanine methyl ester | HCID 13334676 | — |
Reaction Steps
This invention encompasses a method and intermediates for preparing a commercial sweetening agent, α-L-aspartyl-L-phenylalanine methyl ester. The process involves reacting L-aspartic acid with diketene to form N-acetoacetyl-L-aspartic acid which is converted to N-acetoacetyl-L-aspartic anhydride by reaction with acetic anhydride. N-acetoacetyl-L-aspartic anhydride is reacted with L-phenylalanine methyl ester to provide N-acetoacetyl-α-L-aspartyl-L-phenylalanine methyl ester which is converted to α-L-aspartyl-L-phenylalanine methyl ester by reaction with hydroxylamine hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04555362 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-05d9f215620f4c3e98bb5531d5f20502 |
| Source note | uspto-grants-1985_11 |