HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12593Erstellt: 23. Oktober 2026
Bromide ion → (S)-2-(4-bromobenzyl)amino-3-methylbutyric acid
https://huagongshe.com/de/reaction/12593
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bromide ion | HCID 259 | — |
| Edukt | L-Valine | HCID 6287 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (S)-2-(4-bromobenzyl)amino-3-methylbutyric acid | HCID 11673643 | 153,4% |
Reaktionsschritte
52 mL (0.21 mol) of N,O-bistrimethylsilylacetamide is added under nitrogen atmosphere to a mixture made up of 23.5 g (0.20 mol) of L-valine and 38.5 mL (0.22 mol) of diisopropylethylamine in 12.5 mL of DMF. After 1 h at 80° C. the suspension changes to a clear solution. Then, in portions and controlling exothermy, 50 g (0.20 mol) of 4-bromobenzylo bromide is added and left to react at 80° C. for 2 h. The mixture is cooled to 20-25° C., 250 mL of toluene and a solution made up of 250 mL of water and 80 mL of NaOH 40% are added. The resulting aqueous phase is washed twice with 100 mL of AcOEt, the remains of solvent distilled and taken to pH 6-7 with HCl 3N. The solid obtained is filtered with 250 mL of IPA to give 43.9 g (76.5%) of N-(4-bromobenzyl)-L-valine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07728021B2 |
|---|
| Quelldatensatz | uspto-grants-2010_06 |
|---|
| ORD ID | ord-145a239c04c24a43b4d3485f843fcd6d |
|---|
| Quellennotiz | uspto-grants-2010_06 |
|---|