HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sucrose → L-Aspartyl-D-alanine N-(2,2,4,4-tetramethyltetrahydrothiophene-3-yl)amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sucrose | HCID 5988 | — |
| Reactant | (3S)-3-amino-4-[[(2R)-1-amino-1-oxopropan-2-yl]amino]-4-oxobutanoic acid | HCID 11571987 | — |
| Reactant | 3-Amino-2,2,4,4-tetramethyltetrahydrothiophene | HCID 13733567 | — |
| Product | L-Aspartyl-D-alanine N-(2,2,4,4-tetramethyltetrahydrothiophene-3-yl)amide | HCID 13247912 | — |
Reaction Steps
When levorotatory 3-amino-2,2,4,4-tetramethyltetrahydrothiophene, resolved by standard methods, was employed in the above procedure in place of the racemic amine the resulting L-aspartyl-D-alanine amide was found to be 800 times as sweet as sucrose.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04804782 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-fa20bc9e27154a16a777a6cea6761026 |
| Source note | uspto-grants-1989_02 |