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HCID 10030981, Verbindung → HCID 10460748, Verbindung

HRID 482330
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 482330
[Si:1]([O:8][CH2:9][CH2:10][CH2:11][C@H:12]([C@@H:14]1[C@:31]2([CH3:32])[C@H:17]([C@H:18]3[C@H:28]([CH2:29][CH2:30]2)[C@:26]2([CH3:27])[C:21]([CH2:22][C@@H:23]([O:33][CH:34]4[CH2:39][CH2:38][CH2:37][CH2:36][O:35]4)[CH2:24][CH2:25]2)=[CH:20][C:19]3=[O:40])[CH2:16][CH2:15]1)[CH3:13])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]>CCOC(C)=O.[Pt](=O)=O>[Si:1]([O:8][CH2:9][CH2:10][CH2:11][C@H:12]([C@@H:14]1[C@:31]2([CH3:32])[C@H:17]([C@H:18]3[C@H:28]([CH2:29][CH2:30]2)[C@:26]2([CH3:27])[C@H:21]([CH2:22][C@@H:23]([O:33][CH:34]4[CH2:39][CH2:38][CH2:37][CH2:36][O:35]4)[CH2:24][CH2:25]2)[CH2:20][C:19]3=[O:40])[CH2:16][CH2:15]1)[CH3:13])([C:4]([CH3:5])([CH3:6])[CH3:7])([CH3:3])[CH3:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 10030981HCID 10030981, Verbindung

Produkt 1

HCID 10460748HCID 10460748, VerbindungAusbeute 71 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 345198Adams' catalystKatalysatorHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

Compound 2004 (1.0 g, 1.75 mmol) was dissolved in EtOAc (75 ml) and platinum(IV) oxide (0.012 g, 0.049 mmol) was added. The mixture was placed on a hydrogenation apparatus (atmospheric). The set-up was evacuated to remove the dissolved oxygen and then hydrogen was introduced. The evacuation and introduction of hydrogen process was repeated 2 times. The reaction was stirred under hydrogen at atmospheric pressure for 2.5 hours. The reaction mixture was filtered through Celite and concentrated in vacuo. The crude product was purified by flash chromatography (SiO2, hexanes: EtOAc gradient starting with 20:1) giving compound 2005 as a white solid (0.70 g, 71%). 24-t-Butyldimethylsilyloxy-3β-tetrahydropyranyloxy-5α-cholan-7β-ol was obtained as a by-product (21%). (Note: This by-product could be converted to the desired ketone 2005 with Collin's reagent in 64% yield.) Compound 2005: 1H NMR (500 MHz, CDCl3) δ: 4.73-4.66 (m, 1H, THP methine H), 3.95-3.85 (m, 1H, THP CH2O), 3.66-3.52 (m, 3H, THP CH2O & C-24 H), 3.50-3.45 (M, 1H, C-3 H), 1.08 (s, 3H, C-19 H), 0.91 (d, J=6.6 Hz, C-21 H), 0.89 (s, 9H, t-Bu), 0.64 (s, 3H, C-18 H), 0.04 (s, 6H, TBDMS CH3); IR (CHCl3) 2900, 1685 cm-1 ; MS (CI/isobutane) m/z 575 (M+1, 85%), 491 (M+1-THP, 100%); m.p. 166°-170° C.; Anal. calcd. for C35H62 O4SI: C=73.12, H=10.87; Found: C=72.88, H=10.78.

Aufarbeitung

  1. customThe set-up was evacuated
  2. customto remove the dissolved oxygen
  3. additionhydrogen was introduced
  4. filtrationThe reaction mixture was filtered through Celite
  5. concentrationconcentrated in vacuo
  6. customThe crude product was purified by flash chromatography (SiO2, hexanes: EtOAc gradient starting with 20:1)

Quellen und Nachweise

ORD-Eintrag
ord-a647036e08fc4463af9fbe475dfea935
Quelldatensatz
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05795885

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