Ethyl Acetate → 1-(3-Iodophenoxy)-3,6,9-trioxadecane

HRID 128891

반응식

HRID 128891 반응식
CS([O:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][O:14][CH3:15])(=O)=O.[I:16][C:17]1[CH:18]=[C:19](O)[CH:20]=[CH:21][CH:22]=1.C(=O)([O-])[O-].[K+].[K+].CCOC(C)=O>CN(C=O)C.CCCCCC>[I:16][C:17]1[CH:22]=[C:21]([CH:20]=[CH:19][CH:18]=1)[O:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][O:14][CH3:15]

참가 물질

7

반응 조건

온도
68 °C

실험 절차

To a solution of 1-[(methanesulfonyl)-oxy]-3,6,9-trioxadecane (11.6 g, 47.9 mmol) in dry DMF (145 ml) was added 3-iodophenol (10.6 g, 48.2 mmol) and potassium carbonate (6.6 g, 47.8 mmol). The reaction was immersed in an oil bath which was warmed to 68° C. over a period of 0.5 hr. The reaction was stirred at this temperature under an N2 atmosphere for 16 hrs and then at 82° C. for an additional 2 hrs. At the end of this period, the reaction was cooled, diluted with DMF, filtered through a pad of celite and evaporated in vacuo. The resulting residue was taken up into ethyl acetate (500 ml), washed with water (200 ml), 1N aqueous sodium hydroxide (200 ml) and brine (200 ml), dried (Na2SO4), filtered and evaporated in vacuo to provide a light brown oil. Flash column chromatography (silica, 1:3 to 1:2; EtOAc:hexane) provided 1 -(3-iodophenoxy)-3,6,9-trioxadecane as a light yellow oil (10.8 g, 37.1%).

후처리

  1. customThe reaction was immersed in an oil bath
  2. waitat 82° C. for an additional 2 hrs
  3. temperatureAt the end of this period, the reaction was cooled
  4. filtrationfiltered through a pad of celite
  5. customevaporated in vacuo
  6. washwashed with water (200 ml), 1N aqueous sodium hydroxide (200 ml) and brine (200 ml)
  7. dry with materialdried (Na2SO4)
  8. filtrationfiltered
  9. customevaporated in vacuo
  10. customto provide a light brown oil

출처 및 근거

ORD 기록
ord-7e492b043bfe4ec695a995ef1030b663
출처 데이터셋
uspto-grants-1995_11
특허 번호
US05466435

연결된 노트

불러오는 중…