Ammonium Chloride → 1-Chloro-10,14-dimethylnonadeca-10,13-dien-7-yne

HRID 1606681노트

반응식

HRID 1606681 반응식
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]#[CH:9].C([Mg]Br)C.Br[CH2:15][C:16]([CH3:27])=[CH:17][CH2:18][CH:19]=[C:20]([CH3:26])[CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].[Cl-].[NH4+]>CCOCC.O1CCCC1>[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]#[C:9][CH2:15][C:16]([CH3:27])=[CH:17][CH2:18][CH:19]=[C:20]([CH3:26])[CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]

참가 물질

7

실험 절차

A solution of 12.0 g. of 1-chlorooct-7-yne in 20 ml. of tetrahydrofuran is added to a mixture of 27 ml. of 3N ethyl magnesium bromide in ether and 50 ml. of tetrahydrofuran. The mixture is stirred and heated under reflux for 30 min. under nitrogen, then 0.45 g. of powdered cuprous chloride is added and heating and stirring is continued for 20 min. A solution of 20.0 g. of 1-bromo-2,6-dimethyl-2,5-undecadiene in 15-ml. of tetrahydrofuran is added and the mixture is heated under reflux for 10 hrs., then allowed to stand for about 18 hrs., and poured into saturated aqueous ammonium chloride and ether. The mixture is filtered and the ether solution is separated, washed with water, dried over sodium sulfate, and evaporated to leave a residue comprising 1-chloro-10,14-dimethylnonadeca-10,13-dien-7-yne.

후처리

  1. temperatureheated
  2. temperatureunder reflux for 30 min. under nitrogen
  3. temperatureheating
  4. stirringstirring
  5. temperaturethe mixture is heated
  6. temperatureunder reflux for 10 hrs
  7. waitto stand for about 18 hrs
  8. filtrationThe mixture is filtered
  9. customthe ether solution is separated
  10. washwashed with water
  11. dry with materialdried over sodium sulfate
  12. customevaporated

출처 및 근거

ORD 기록
ord-0cca801f0c7d4f3499e42b514095badf
출처 데이터셋
uspto-grants-1976_04
특허 번호
US03953499

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