HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1643405Erstellt: 25. Oktober 2026
Ethyl Acetate → (S)-tert-butyl 5,6-dihydroxyhexanoate
https://huagongshe.com/reaction/1643405
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Sodium Pyrosulfite | HCID 656671 | — |
| Edukt | Tert-butyl hex-5-enoate | HCID 15047738 | — |
| Edukt | Water butanol | HCID 22253497 | — |
| Edukt | 1-((1R)-((2R,4R,5S)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methoxy)-4-((1R)-((2R,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methoxy)phthalazine | HCID 51003674 | — |
| Produkt | (S)-tert-butyl 5,6-dihydroxyhexanoate | HCID 58209443 | — |
Reaktionsschritte
To a suspension of AD-mix-α (70 g) in water/butanol 1:1 (512 mL) cooled to 0° C., tert-butyl hex-5-enoate (8.5 g, 49.92 mmol) was added. The reaction mixture was stirred at 4° C. for 70 hrs. Then the reaction mixture was cooled to 0° C. and EtOAc (280 mL), followed by continuous portionwise addition of sodium metabisulfite (20.6 g). The mixture was stirred for 30 min at 0° C. and at rt for 1 hour. The organic layer was separated and the aqueous phase extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. Chromatography over silica gel eluting with EtOAc 100% afforded the title compound as a pale yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08119806B2 |
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| Quelldatensatz | uspto-grants-2012_02 |
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| ORD ID | ord-13b28ff0e5b845a0bd86d1e91e31ebc1 |
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| Quellennotiz | uspto-grants-2012_02 |
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