HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178418361, compound → D-Glutamic acid, 4-hydroxy-4-(1H-indol-3-ylmethyl)-, (4S)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | 4-Hydroxy-4-(3-indolylmethyl)-2-hydroxyiminoglutarate ammonium salt | HCID 178525499 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Water | HCID 962 | — |
| Product | D-Glutamic acid, 4-hydroxy-4-(1H-indol-3-ylmethyl)-, (4S)- | HCID 9814579 | — |
| Product | D-Glutamic acid, 4-hydroxy-4-(1H-indol-3-ylmethyl)-, (4R)- | HCID 9922096 | — |
Reaction Steps
1.0 g (2.94 mmol) of 4-hydroxy-4-(3-indolylmethyl)-2-hydroxyiminoglutarate ammonium salt was dissolved in 10 ml of water, to which 1 ml of a Raney-nickel catalyst (manufactured by Kawaken Fine Chemicals Co., Ltd.; developed nickel catalyst NDHT-90) was added with a syringe, and the mixture stirred at a hydrogen pressure of 20 atmospheres for 10 hours. The catalyst was filtered off, and the resulting solution was concentrated to obtain the residue. The residue was analyzed by NMR. It was shown that 0.29 g (0.89 mmol; yield, 30%) of (2S,4S)/(2R,4R)-4-hydroxy-4-(3-indolylmethyl)-2-aminoglutaric acid (monatin) and 0.29 g (0.89 mmol; yield, 30%) of (2S,4R)/(2R,4S)-4-hydroxy-4-(3-indolylmethyl)-2-aminoglutaric acid were generated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678925B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-d574697b4cae47d382a45714c30a3689 |
| Source note | uspto-grants-2010_03 |