HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921493Generated: October 31, 2026
Ammonia → (S)-Benzyl-3-hydroxyglutaramate
https://huagongshe.com/reaction/921493
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| Reactant | (S)-methyl-3-hydroxyglutaramate | HCID 10725662 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Isopropyl Acetate | HCID 7915 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | (S)-Benzyl-3-hydroxyglutaramate | HCID 89601064 | — |
Reaction Steps
Mixture of Benzyl alcohol (131.0 g), (S)-methyl-3-hydroxyglutaramate (100 g) and Tetraisopropyl orthotitanate (17.5 g) are mixed in a flask. The mixture was stirred under vacuum at 50-60° C. for about 5 hrs. The reaction mixture was cooled and diluted with isopropyl acetate (500 ml). The reaction mixture was added to a stirred solution of Tartaric acid (37 g in 370 ml DM water) and 500 ml isopropyl acetate mixture. The reaction mixture was stirred and pH was adjusted to 7.0-8.0 by Aq ammonia solution. Layers were separated. The organic phase was removed and the aqueous phase was extracted with isopropyl acetate. Combined organic layer was washed with Aq ammonia and tartaric acid solution followed by brine wash. The organic phase was dried over anhydrous sodium sulphate and evaporated under reduced pressure to yield oil. To this oil tert-butyl methyl ether (800 ml) was added, stirred, cooled, filtered and dried to give (S)-Benzyl-3-hydroxyglutaramate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09273333B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-7ad0e6007a2f48d49c85a2bea7e114bd |
|---|
| Source note | uspto-grants-2016_03 |
|---|