HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1172992Erstellt: 25. Oktober 2026
Sodium Hydroxide → 3-Methyl-3,4-dihydro-2H-1,4-benzoxazine
https://huagongshe.com/reaction/1172992
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2H-1,4-benzoxazin-3(4H)-one | HCID 72757 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | HCID 178418332 | HCID 178418332 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 3-Methyl-3,4-dihydro-2H-1,4-benzoxazine | HCID 2763760 | 46% |
Reaktionsschritte
To a solution of 2H-1,4-benzoxazin-3(4H)-one (2.00 g, 13.4 mmol) in tetrahydrofuran (20 ml) was added dropwise at 5° C. a THF solution of methylmagnesium chloride (17.9 ml, 3 M, 53.7 mmol) and the reaction mixture was then stirred at 50° C. for 90 min. The reaction mixture was then cooled to 5° C. and quenched by dropwise addition of 20 ml acetic acid. Sodium borohydride (1.27 g, 33.5 mmol) was then added portionwise and the mixture was stirred at room temperature overnight. The resulting suspension was then cooled to 0° C. and 3 N aq. sodium hydroxide solution was added dropwise until the mixture was pH 10. Ethyl acetate was then added, the phases separated, and the organic phase dried over sodium sulphate and concentrated in vacuo. The residue was purified by chromatography on silica gel (eluant: heptane/ethyl acetate gradient) to yield the title compound as a colorless oil (0.92 g, 46%); MS (ISP): 150.3 ([M+H]+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07834044B2 |
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| Quelldatensatz | uspto-grants-2010_11 |
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| ORD ID | ord-4f5fa2ca77274077b24abc3683f37896 |
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| Quellennotiz | uspto-grants-2010_11 |
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