HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1772307Erstellt: 24. Oktober 2026
(S)-beta-Benzoyloxy-gamma-butyrolactone → 3-O-benzoyl-2-deoxy-threose
https://huagongshe.com/de/reaction/1772307
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | (S)-beta-Benzoyloxy-gamma-butyrolactone | HCID 10058799 | — |
| Edukt | Diisopropylaluminium hydride | HCID 21896610 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-O-benzoyl-2-deoxy-threose | HCID 86664513 | 75% |
Reaktionsschritte
To a solution of 101 (0.780 g, 3.8 mmol) in 13 mL dry THF was slowly dropwise added 1.0 M diisopropyl aluminiumhydride (4.7 mL, 4.7 mmol) in toluene at −78° C. The reaction mixture was stirred at −78° C., and as soon as the material was completely consumed (TLC, 2 hours), methanol (2 mL) was slowly added in order to quench the reaction. The cooling bath was removed, 15 mL of a saturated ageous sodium potassium tartrate solution and 25 mL of EtOAc were added and the mixture stirred vigorously for 3 hours. The organic layer was washed with water and brine, and concentrated under vacuo. The residue was purified by chromatography on a silica gel column (n-hexane/EtOAc=8:2) to afford 102 (590 mg, 2.8 mmol) as a colorless oil, in 75% yield, which was characterized as follows:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09249177B2 |
|---|
| Quelldatensatz | uspto-grants-2016_02 |
|---|
| ORD ID | ord-35fd35b6a3b440b094a36b4ccde6bc19 |
|---|
| Quellennotiz | uspto-grants-2016_02 |
|---|