Hydrochloric Acid → 7,8-Difluorochroman-6-ol

HRID 2244829노트

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HRID 2244829 반응식
[Li]CCCC.[F:6][C:7]1[C:16]([F:17])=[C:15]2[C:10]([CH2:11][CH2:12][CH2:13][O:14]2)=[CH:9][CH:8]=1.B(OC)(OC)[O:19]C.OO.Cl>C1COCC1.O.C(O)(=O)C>[F:6][C:7]1[C:16]([F:17])=[C:15]2[C:10]([CH2:11][CH2:12][CH2:13][O:14]2)=[CH:9][C:8]=1[OH:19]

참가 물질

9

실험 절차

81.2 ml (0.13 mol) of n-BuLi (15% soln. in hexane) are added at −70° C. to a soln. of 20.0 g (0.12 mol) of 7,8-difluorochroman in 400 ml of THF. After 3 h at this temperature, 14.4 ml (0.13 mol) of trimethyl borate are added dropwise, and the batch is warmed to room temperature. 30 ml of dilute acetic acid (about 30%) are added, and 30 ml of aq. hydrogen peroxide soln. (35%) are carefully added to the batch. When the addition is complete, the mixture is stirred at 20° C. for 17 h. Water is added, and the batch is acidified using HCl. The solution is extracted a number of times with MTBE, and the combined organic phases are washed successively with water, sat. sodium chloride soln. and ammonium iron(II) sulfate soln. The solution is dried using sodium sulfate and concentrated to dryness. The crude product is purified by column chromatography (SiO2, n-heptane:MTBE=2:1).

후처리

  1. addition(35%) are carefully added to the batch
  2. additionWhen the addition
  3. extractionThe solution is extracted a number of times with MTBE
  4. washthe combined organic phases are washed successively with water, sat. sodium chloride soln
  5. customThe solution is dried
  6. concentrationconcentrated to dryness
  7. customThe crude product is purified by column chromatography (SiO2, n-heptane:MTBE=2:1)

출처 및 근거

ORD 기록
ord-808ffefdfee94112b52765574e028683
출처 데이터셋
uspto-grants-2010_03
특허 번호
US07678929B2

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