HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21767Erstellt: 23. Oktober 2026
Sulfuric Acid → 3-Methyl-5-(1-methyl-2(S)-pyrrolidinyl)isoxazole
https://huagongshe.com/de/reaction/21767
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Benzyloxycarbonyl-L-proline | HCID 101987 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-Methyl-5-(1-methyl-2(S)-pyrrolidinyl)isoxazole | HCID 119380 | 88% |
Reaktionsschritte
To a stirred suspension of sodium borohydride (7.59 g, 200 mmol) in 100 mL of THF cooled to 0° C. was added a solution of 20 g (80.28 mmol) of N-Cbz-L-proline, from step 24a above, in 50 mL of ether. To this solution was added dropwise a solution of 5 mL of H2SO4 in 20 mL of ether, with stirring and while maintaining the temperature below 20° C. The reaction mixture was warmed to room temperature and stirred for 16 hr. The reaction was quenched by the addition of 100 mL of methanol dropwise. The solvents were removed, 30 mL of 4N NaOH was added, and the mixture was extracted with ethyl acetate. The organic extract was dried over Na2SO4 and concentrated to afford the title product, 16.61 g (88 % yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05424444 |
|---|
| Quelldatensatz | uspto-grants-1995_06 |
|---|
| ORD ID | ord-c9a6f38691244cecb730d2b45b58285c |
|---|
| Quellennotiz | uspto-grants-1995_06 |
|---|