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HRID 1107198Erstellt: 25. Oktober 2026
Estra-1,3,5(10),16-tetraen-6-one-3-yl acetate → Estra-1,3,5(10),16-tetraen-3,6-diol
https://huagongshe.com/reaction/1107198
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Estra-1,3,5(10),16-tetraen-6-one-3-yl acetate | HCID 15870994 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Edukt | Estra-1,3,5(10),16-tetraen-6-one-3-yl-acetate | HCID 22873077 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Estra-1,3,5(10),16-tetraen-3,6-diol | HCID 15870995 | 10% |
Reaktionsschritte
To a suspension of lithium aluminum hydride (LAH, 95%, 46.9 mg, 1.17 mmol) in 5 ml of anhydrous THF was added estra-1,3,5(10),16-tetraen-6-one-3-yl acetate, 6 (422.9 mg, 1.360 mmol) in 5 ml of anhydrous THF dropwise, with stirring. See FIG. 156. The reaction was stirred 50 min., after which further LAH (46.5 mg, 1.16 mmol) was added and the reaction stirred 22 h. After refluxing 4 h TLC still showed starting material. The reaction was quenched with 0.5 ml of water+0.5 ml of 20% (w/w) sulfuric acid and concentrated under reduced pressure. The residue was extracted four times with 10 ml portions of hot ethyl acetate and filtered through Celite. The combined filtrates were concentrated and purified twice by flash chromatography to give solid product (0.05 g, 0.2 mmol, 10%), m.p. 150-157° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06057439 |
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| Quelldatensatz | uspto-grants-2000_05 |
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| ORD ID | ord-6485720089a0499ea745ec346d9675ff |
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| Quellennotiz | uspto-grants-2000_05 |
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