Réaction #428043

ord-7d28b922d3514bfab34b3e18eaf014da

Équation de réaction

CC(=O)OC(C)=O
Acetic anhydride
CC(C)(O)CCO
3-methylbutane-1,3-diol
CC(=O)OCCC(C)(C)O
3-Hydroxy-3-methylbutyl acetate

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagethe solution was washed with 10% aqueous ammonium chloride (2×20 mL), 5% sodium carbonate (2×20 mL) and brine (1×20 mL)
  2. 2
    Séchagedried over sodium sulfate
  3. 3
    Autreevaporated to dryness
  4. 4
    Autreto yield a clear, yellow liquid

Mode opératoire

A solution of 16 mL 3-methylbutane-1,3-diol in 10 mL methylene chloride with a catalytic amount of 4-dimethylpyridine was cooled to 0° C. Acetic anhydride (4.084 g, 40 mmol) was then added drop wise and the solution was stirred for 5 hours. An additional 10 mL of methylene chloride was added and the solution was washed with 10% aqueous ammonium chloride (2×20 mL), 5% sodium carbonate (2×20 mL) and brine (1×20 mL), dried over sodium sulfate and evaporated to dryness to yield a clear, yellow liquid. (2.402 g) 1H NMR (400 MHz, CDCl3): δ 1.24 (s, 6H), 1.56 (b, 1H), 1.80-1.83 (t, J=6.8, 2H), 2.02 (s, 3H), 4.22 (t, J=6.9, 2H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08895691B2uspto-grants-2014_11