Reaktion #1808710

ord-06d285a44fc04e99a54b88fb3cc8b653

Reaktionsgleichung

C=C1CC[C@H](O)C/C1=C/C=C1\CCC[C@]2(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@@H]12
dihydrocholesterol
O=C(O)c1ccccc1I(=O)=O
o-iodoxybenzoic acid
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
5α-cholestan-3-one
Ausbeute 89.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter 2 hr precipitation of a white solid
  2. 2
    workup.ADDITIONAfter 5 hr the reaction solution was poured into Na2CO3 (5%, 40 ml)
  3. 3
    Extraktionextracted with diethyl ether/n-hexane (50:50; 3×30 ml)
  4. 4
    WaschenThe combined organic layers were washed with water (2×15 ml)
  5. 5
    Trocknendried over sodium sulfate
  6. 6
    SonstigeThe residue was crystallised from ethanol

Vorschrift

A solution of dihydrocholesterol (1.94 g; 5 mmol) in THF (8 ml) was added to a solution of o-iodoxybenzoic acid I (2.10 g, 7.5 mmol) in DMSO (14 ml). After 2 hr precipitation of a white solid was observed. After 5 hr the reaction solution was poured into Na2CO3 (5%, 40 ml) and extracted with diethyl ether/n-hexane (50:50; 3×30 ml). The combined organic layers were washed with water (2×15 ml), dried over sodium sulfate and brought to dryness under vacuum. The residue was crystallised from ethanol to give 1.73 g (89%) of 5α-cholestan-3-one mp 129°-130° C. (lit. 128°-130° C.: Beilsteins Handbuch der organischen Chemie, III E., 7, 1330b).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05510538uspto-grants-1996_04