HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Phenylalanine → HCID 10977466, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 10888355 | HCID 10888355 | — |
| Product | HCID 10977466 | HCID 10977466 | — |
Reaction Steps
A method of preparing α-APM derivatives without using an expensive L-phenylalanine is provided, wherein 2,5-dioxopiperazine-3-acetamide is reacted with acetic anhydride to give N,N'-diacetyl-6-cyanomethyl-2,5-dioxopiperazine, which is then reacted with benzaldehyde in the presence of a strong base to give 1-acetyl-3-benzylidene-6-cyanomethyl-2,5-dioxopiperazine. This is treated with hydrazine to give 3-benzylidene-6-cyanomethyl-2,5-dioxopiperazine, which is then reduced to prepare 3-benzyl-6-cyanomethyl-2,5-dioxopiperazine, which is converted by reaction with methanol in the presence of a strong acid to an α-APM derivative for use as a sweetener.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294714 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-3e32e99d8c4f40ada791a3c6a0d9d410 |
| Source note | uspto-grants-1994_03 |