反応 #1563893

ord-82b151e0d5db4839be88b0419976a20c

反応方程式

CCCCCC=CCC=CCCCCCCCCCC(=O)O
11,14-Eicosadienoic acid
CNOC.Cl
N,O-Dimethylhydroxylamine hydrochloride
On1nnc2cccnc21
HOAt
CCN(CC)CC
Et3N
ClCCCl
EDC
CCCCCC=CCC=CCCCCCCCCCC(N)=O
11,14-eicosadienamide
収率 93.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他Reaction
  2. 2
    洗浄was then washed 5×700 mL water
  3. 3
    洗浄washed 1×600 mL 1 M NaOH
  4. 4
    乾燥dried with sodium sulfate
  5. 5
    ろ過filtered through celite
  6. 6
    その他evaporated

実験手順

11,14-Eicosadienoic acid, (11Z,14Z)- (50 g, 162 mmol), N,O-Dimethylhydroxylamine hydrochloride (31.6 g, 324 mmol), HOAt (44.1 g, 324 mmol), Et3N (45.2 mL, 324 mmol), and EDC (62.1 g, 324 mmol) were mixed in DCM (810 mL) and stirred overnight at ambient temperature. Reaction was then washed 5×700 mL water, then washed 1×600 mL 1 M NaOH, dried with sodium sulfate, filtered through celite and evaporated to obtain 53.06 g (93%) 11,14-eicosadienamide, N-methoxy-N-methyl-, (11Z,14Z) as a clear golden oil. 1H NMR (400 MHz, CDCl3) δ 5.35 (m, 4H), 3.68 (s, 3H), 3.18 (s, 3H), 2.77 (m, 2H), 2.41 (t, J=7 Hz, 2H), 2.05 (m, 4H), 1.63 (m, 2H), 1.40-1.26 (m, 18H), 0.89 (t, J=7 Hz, 3H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09402816B2uspto-grants-2016_08