Réaction #452814

ord-199c474a196e4bd9839f8c11963e69b3

Équation de réaction

CC12CC3CC(C)(C1)CC(Br)(C3)C2
3,5-dimethyl-1-bromoadamantane
CC(=O)[O-].[K+]
potassium acetate
CC(=O)OC12CC3CC(C)(CC(C)(C3)C1)C2
desired product
CC(=O)OC12CC3CC(C)(CC(C)(C3)C1)C2
3,5-dimethyl-1-adamantyl acetate

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionextracted with 3×10 mL of diethyl ether
  2. 2
    LavageThe combined ether extracts are washed with saturated aqueous sodium bicarbonate
  3. 3
    Séchagedried over sodium sulfate
  4. 4
    AutreThe solvent is removed under vacuum

Mode opératoire

2.486 (10.2 mmoles) of 3,5-dimethyl-1-bromoadamantane is refluxed for 16 hours with 2.034 g (20.7 mmoles) of potassium acetate in 10 mL of acetic acid. The solution is poured over 100 grams of ice, allowed to melt, and extracted with 3×10 mL of diethyl ether. The combined ether extracts are washed with saturated aqueous sodium bicarbonate followed by saturated aqueous sodium chloride, then dried over sodium sulfate. The solvent is removed under vacuum, yielding 1.521 (67%) of the desired product, a colorless oil. TLC: Rf=0.68 (silica plate: eluant hexane 90%, ethyl acetate 10%). 1HNMR (CDCl3, 500 Mhz): 0.858 (s, 6H), 1.115 (d, 2H, J=12.4 Hz), 1.177 (d, 2H, J=12.4 Hz), 1.260 (d, 2H, J=12.3 Hz), 1.367 (d, 2H, J=12.3 Hz), 1.714 (d, 2H, J=11.6 Hz), 1.766 (d, 2H, J=11.6 Hz), 1.939 (s, 2H), 1.976 (s, 3H), 2.191 (m, 1H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06127415uspto-grants-2000_10