Hippuristanol → HCID 49864735, Verbindung

HRID 1677836Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1677836
[CH3:1][C@@H:2]1[C:31]([CH3:33])([CH3:32])[O:30][C@:4]2([O:8][C@H:7]3[CH2:9][C@H:10]4[C@@H:15]5[CH2:16][CH2:17][C@H:18]6[CH2:23][C@H:22]([OH:24])[CH2:21][CH2:20][C@:19]6([CH3:25])[C@H:14]5[C@@H:13]([OH:26])[CH2:12][C@:11]4([CH3:27])[C@H:6]3[C@:5]2([OH:29])[CH3:28])[CH2:3]1>N1C=CC=CC=1.O=[Cr](=O)(O[Cr](=O)([O-])=O)[O-].[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.CCOCC>[CH3:1][C@@H:2]1[C:31]([CH3:32])([CH3:33])[O:30][C@:4]2([O:8][C@H:7]3[CH2:9][C@H:10]4[C@@H:15]5[CH2:16][CH2:17][C@H:18]6[CH2:23][C@H:22]([OH:24])[CH2:21][CH2:20][C@:19]6([CH3:25])[C@H:14]5[C:13](=[O:26])[CH2:12][C@:11]4([CH3:27])[C@H:6]3[C@:5]2([OH:29])[CH3:28])[CH2:3]1.[CH3:1][C@@H:2]1[C:31]([CH3:32])([CH3:33])[O:30][C@:4]2([O:8][C@H:7]3[CH2:9][C@H:10]4[C@@H:15]5[CH2:16][CH2:17][C@H:18]6[CH2:23][C:22](=[O:24])[CH2:21][CH2:20][C@:19]6([CH3:25])[C@H:14]5[C:13](=[O:26])[CH2:12][C@:11]4([CH3:27])[C@H:6]3[C@:5]2([OH:29])[CH3:28])[CH2:3]1

Komponenten

6

Edukt 1

HCID 9981822Hippuristanol

Produkt 2

HCID 49864734HCID 49864734, VerbindungAusbeute 28 %HCID 49864735HCID 49864735, VerbindungAusbeute 56 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 1049PyridineLösungsmittelHCID 3283Diethyl EtherLösungsmittelHCID 2724130Cornforth reagentLösungsmittel

Versuchsvorschrift

Oxidation of hippuristanol (1) to yield hippuristanol 11-one (4) and hippuristanol 3, 11-dione (5). To an ice-cooled solution of hippuristanol (1, 31.7 mg) in pyridine (0.5 mL), Cornforth reagent (0.7 mL) was added dropwise. The mixture was kept stirring for 30 min. in an ice bath, then 3 hr at RT. The mixture was taken up in ether and the suspension was filtered. The filtrate was washed with dilute hydrochloric acid, dried over Na2SO4, and concentrated. The resulting product was separated on silica TLC (CHCl3/EtOAc, 3:1, v/v) to give 8.8 mg of hippuristanol 11-one (4, 28%) and 17.7 mg of hippuristanol 3,11-dione (5, 56%). Hippuristanol 3,11-dione (5). white crystals. mp 181-183.5° C.; 1H NMR (CDCl3) δ 4.42 (m, 2H), 3.02 (s, 1H), 2.82 (ddd, J=13.0, 6.5, 2.0 Hz, 1H), 2.63 (d, J=12.0 Hz, 1H), 2.45 (dt, J=6.5, 14.5 Hz, 1H), 2.37 (dd, J=13.0, 8.0 Hz, 1H), 1.31 (s, 3H), 1.22 (s, 6H), 1.20 (s, 3H), 1.11 (s, 3H), 0.99 (d, J=7.0 Hz, 3H); 13C NMR (CDCl3) δ 211.6, 210.0, 115.0, 84.9, 80.4, 79.1, 63.9, 63.4, 58.8, 54.5, 46.9, 46.3, 44.3, 41.8, 40.5, 38.0, 37.0, 35.5, 35.2, 33.7, 32.4, 28.7, 28.5, 28.2, 23.0, 17.3, 14.8, 11.0; IR (KBr) 3510, 1695 cm−1; EIMS m/z 458 (M+, 5), 316 (92), 84 (100%).

Aufarbeitung

  1. additionwas added dropwise
  2. custom3 hr
  3. customat RT
  4. filtrationthe suspension was filtered
  5. washThe filtrate was washed with dilute hydrochloric acid
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. customThe resulting product was separated on silica TLC (CHCl3/EtOAc, 3:1

Quellen und Nachweise

ORD-Eintrag
ord-c35980a653c54caf8eb75a8521aa20ad
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US08008346B2

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