Réaction #324362

ord-99f9bf9f4c87431086396d9442f22e04

Équation de réaction

CCCCCCCCCCCCNCCCCCCCCCCCC
didodecylamine
CCCCCCCCCCCCNCCCCCCCCCCCC
N,N-didodecylamine
CCN(C(C)C)C(C)C
diisopropylethylamine
C=CC(=O)Cl
acryloyl chloride
C=CC(=O)N(CCCCCCCCCCCC)CCCCCCCCCCCC
product 71
C=CC(=O)N(CCCCCCCCCCCC)CCCCCCCCCCCC
N,N-Didodecylacrylamide

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONAfter the completion of the addition the reaction mixture
  2. 2
    Autrethe completion of the reaction
  3. 3
    LavageThe reaction mixture was washed with satd
  4. 4
    SéchageNaHCO3 solution (200 mL), water (200 mL), brine (100 mL) and dried over NaSO4

Mode opératoire

To a solution of didodecylamine 66 (25 g, 70 7 mmol) and diisopropylethylamine (18 g, 141 mmol) in anhydrous CH2Cl2 (700 mL) at −10° C., a solution of acryloyl chloride (7.68 g, 85 mmol) in CH2Cl2 (100 mL) was added dropwise over a period of 20 min. After the completion of the addition the reaction mixture was stirred for 4 h at 0° C. after which the TLC of the reaction mixture showed the completion of the reaction. The reaction mixture was washed with satd. NaHCO3 solution (200 mL), water (200 mL), brine (100 mL) and dried over NaSO4. Concentration of the organic layer provided the product 71 (28.4 g, 100%) which was used as such in the next step. 1H NMR CDCl3 δ 0.94 (t, J=6.5 Hz, 6H), 1.05-1.69 (m, 40H), 3.15-3.60 (dt, 4H), 5.64 (d, 1H), 6.36 (d, 1H), 6.63 (m, 1H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08642076B2uspto-grants-2014_02