Hexane → HCID 22226108, 화합물

HRID 1744913노트

반응식

HRID 1744913 반응식
[H-].C([Al+]CC(C)C)C(C)C.CCCCCC.[CH2:17]([O:20][C:21]1[C:22](/[C:35](/[CH2:43][CH3:44])=[C:36](/[F:42])\[C:37](OCC)=[O:38])=[CH:23][C:24]2[C:25]([CH3:34])([CH3:33])[CH2:26][CH2:27][C:28]([CH3:32])([CH3:31])[C:29]=2[CH:30]=1)[CH2:18][CH3:19]>C1COCC1>[CH2:17]([O:20][C:21]1[C:22](/[C:35](/[CH2:43][CH3:44])=[C:36](/[F:42])\[CH2:37][OH:38])=[CH:23][C:24]2[C:25]([CH3:33])([CH3:34])[CH2:26][CH2:27][C:28]([CH3:32])([CH3:31])[C:29]=2[CH:30]=1)[CH2:18][CH3:19]

참가 물질

5

반응 조건

온도
-78 °C

실험 절차

A solution of diisobutylaluminum hydride and hexane (40 mL, 1 M, 40 mmol) was added to a stirring solution of ethyl (E)-3-(3-n-propoxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-2-fluoropent-2-enoate (Intermediate 8, 3.52 g, 9.36 mmol) in THF (60 mL) at −78° C. under argon. The solution was stirred at −78° C. for 3 h, and the reaction was quenched at −78° C. by adding methanol. The solution was warmed to room temperature and stirred for 1.5 h. The solution was treated with 1 M aqueous HCl, and the products were extracted three times with ether. The combined organic layers were washed with water, brine and dried over magnesium sulfate. The solvent was removed in vacuo to give the title compound after purification by silica gel chromatography (15% ethyl acetate in hexane).

후처리

  1. customthe reaction was quenched at −78° C.
  2. additionby adding methanol
  3. temperatureThe solution was warmed to room temperature
  4. stirringstirred for 1.5 h
  5. additionThe solution was treated with 1 M aqueous HCl
  6. extractionthe products were extracted three times with ether
  7. washThe combined organic layers were washed with water, brine
  8. dry with materialdried over magnesium sulfate
  9. customThe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-e3151f77ef8147949ba5296e949ae547
출처 데이터셋
uspto-grants-2006_03
특허 번호
US07019034B2

반응 노트

불러오는 중…