Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252665Generated: October 26, 2026

2-Hydroxy-2-[(1H-indol-3-yl)methyl]-4-(methoxyimino)pentanedioic acid → D-Glutamic acid, 4-hydroxy-4-(1H-indol-3-ylmethyl)-, (4S)-

https://huagongshe.com/reaction/252665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxy-2-[(1H-indol-3-yl)methyl]-4-(methoxyimino)pentanedioic acidHCID 71441303—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178503043HCID 178503043—
SolventAmmoniaHCID 222—
ProductD-Glutamic acid, 4-hydroxy-4-(1H-indol-3-ylmethyl)-, (4S)-HCID 9814579—
ProductD-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868187B2
Source datasetuspto-grants-2011_01
ORD IDord-cb18537b5e1f4bdf8a323aee0371b1a5
Source noteuspto-grants-2011_01