Iodine → 7,8-Difluoro-5-iodo-6-methoxymethoxy-2-pentylchroman

HRID 2244840노트

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HRID 2244840 반응식
[F:1][C:2]1[C:11]([F:12])=[C:10]2[C:5]([CH2:6][CH2:7][CH:8]([CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[O:9]2)=[CH:4][C:3]=1[O:18][CH2:19][O:20][CH3:21].[Li]CCCC.[I:27]I.S([O-])(O)=O.[Na+]>C1COCC1.CC(OC)(C)C>[F:1][C:2]1[C:11]([F:12])=[C:10]2[C:5]([CH2:6][CH2:7][CH:8]([CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[O:9]2)=[C:4]([I:27])[C:3]=1[O:18][CH2:19][O:20][CH3:21]

참가 물질

7

실험 절차

17.7 g (58.9 mmol) of 7,8-difluoro-6-methoxymethoxy-2-pentylchroman are initially introduced in 370 ml of THF, and 47.7 ml (75.9 mmol) of n-BuLi (15% soln. in hexane) are added dropwise at −78° C. When the addition is complete, the mixture is stirred at this temperature for 30 min and subsequently at room temperature for 1 h. The solution is re-cooled to −78° C., and a solution of 17.9 g (70.7 mol) of iodine in 100 ml of THF is added dropwise. The reaction mixture is stirred at room temperature for 90 min and subsequently diluted with MTBE. Sat. sodium hydrogensulfite soln. is added to the mixture, which is subsequently washed with water and sat. sodium chloride soln. The crude product remaining after drying using sodium sulfate and removal of the solvents is purified by column chromatography (SiO2, n-heptane:MTBE=3:1), giving 7,8-difluoro-5-iodo-6-methoxymethoxy-2-pentylchroman as a brown oil.

후처리

  1. additionWhen the addition
  2. temperatureThe solution is re-cooled to −78° C.
  3. stirringThe reaction mixture is stirred at room temperature for 90 min
  4. additionis added to the mixture, which
  5. washis subsequently washed with water and sat. sodium chloride soln
  6. customafter drying
  7. customsodium sulfate and removal of the solvents
  8. customis purified by column chromatography (SiO2, n-heptane:MTBE=3:1)

출처 및 근거

ORD 기록
ord-ac281643d9814b7fac09eece3ac33200
출처 데이터셋
uspto-grants-2010_03
특허 번호
US07678929B2

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