1,2-Dichloroethane → 11,14-Eicosadienamide

HRID 64509Notes

Reaction equation

HRID 64509 reaction equation
[C:1]([OH:22])(=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH:11]=[CH:12][CH2:13][CH:14]=[CH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20].Cl.C[NH:25]OC.C1C=NC2N(O)N=NC=2C=1.CCN(CC)CC.C(Cl)CCl>C(Cl)Cl>[C:1]([NH2:25])(=[O:22])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH:11]=[CH:12][CH2:13][CH:14]=[CH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]

Participants

7

Procedure

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 1M 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.

Workup

  1. customReaction
  2. washwas then washed 5×700 mL water
  3. washwashed 1× 600 mL 1M NaOH
  4. dry with materialdried with sodium sulfate
  5. filtrationfiltered through celite
  6. customevaporated

Sources & evidence

ORD record
ord-6f1b0f4d6d5248df9e5fcb23777a5ae7
Source dataset
uspto-grants-2016_09
Patent number
US09447420B2

Reaction notes

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