Reaktion #449952

ord-d70439b6864748c199214ca0aa8eab5e

Reaktionsgleichung

CC(=O)OCCl
chloromethyl acetate
CC(=O)Cl
acetyl chloride
C=O
formaldehyde
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
dehydroepiandrosterone
[H-].[Na+]
sodium hydride
[H-].[Na+]
sodium hydride
→
CC(=O)O.C[C@]12CC[C@H](OCO)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
desired compound
CC(=O)O.C[C@]12CC[C@H](OCO)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
3β-hydroxymethoxy-5androsten-17-one acetate

Edukte

CC(=O)OCCl
chloromethyl acetate
CC(=O)Cl
acetyl chloride
C=O
formaldehyde
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
dehydroepiandrosterone
[H-].[Na+]
sodium hydride
[H-].[Na+]
sodium hydride

Reagenzien

[Cl-].[Cl-].[Zn+2]
ZnCl2

Lösungsmittel

O
water
C1CCOC1
THF

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONis added
  2. 2
    Temperaturthe mixture is heated for a few hours
  3. 3
    TemperaturAfter cooling
  4. 4
    Extraktionextracted with ethyl acetate
  5. 5
    WaschenThe organic phase is then washed with water
  6. 6
    Sonstigedried
  7. 7
    Filtrationfiltered
  8. 8
    Sonstigeevaporated to dryness

Vorschrift

To a solution of dehydroepiandrosterone (2.88 g, 10 mmol) in THF (100 mL) is added sodium hydride (11 mmol, 60% in oil) at room temperature under an argon atmosphere. When all the sodium hydride has reacted, chloromethyl acetate (prepared from acetyl chloride and formaldehyde (or derivative) using ZnCl2 as catalyst) is added and the mixture is heated for a few hours. After cooling, the mixture is poured into water and extracted with ethyl acetate. The organic phase is then washed with water, dried, filtered and evaporated to dryness to give the desired compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05872114uspto-grants-1999_02