HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Hydroxy-2-[(1H-indol-3-yl)methyl]-4-(methoxyimino)pentanedioic acid → D-Glutamic acid, 4-hydroxy-4-(1H-indol-3-ylmethyl)-, (4S)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Hydroxy-2-[(1H-indol-3-yl)methyl]-4-(methoxyimino)pentanedioic acid | HCID 71441303 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178503043 | HCID 178503043 | — |
| Solvent | Ammonia | HCID 222 | — |
| 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
0.264 g (0.824 mmol) of 4-hydroxy-4-(3-indolylmethyl)-2-methoxyiminoglutaric acid was dissolved in 10 ml of aqueous 28% ammonia. 0.18 g of 5% rhodium carbon (dry product) was added and the mixture stirred at a hydrogen pressure of 7.5 atmospheres for 18 hours. The catalyst was filtered off and the solvent was distilled off under reduced pressure, to obtain the residue. The resulting residue was analyzed by NMR, and a mixture of 0.115 g (0.395 mmol; yield, 48%) of (2S, 4S)/(2R, 4R)-4-hydroxy-4-(3-indolylmethyl)-2-aminoglutaric acid (monatin) and 0.065 g (0.223 mmol; yield, 27%) of (2S, 4R)/(2R, 4S)-4-hydroxy-4-(3-indolylmethyl)-2-aminoglutaric acid was found to have been generated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07868187B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-cb18537b5e1f4bdf8a323aee0371b1a5 |
| Source note | uspto-grants-2011_01 |