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Hydrochloric Acid → 7,8-Difluoro-5-iodo-2-pentylchroman-6-ol

HRID 2244841
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HRID 2244841 반응식
Cl.[F:2][C:3]1[C:12]([F:13])=[C:11]2[C:6]([CH2:7][CH2:8][CH:9]([CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[O:10]2)=[C:5]([I:19])[C:4]=1[O:20]COC>C1COCC1.CC(OC)(C)C>[F:2][C:3]1[C:12]([F:13])=[C:11]2[C:6]([CH2:7][CH2:8][CH:9]([CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[O:10]2)=[C:5]([I:19])[C:4]=1[OH:20]
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참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 592152607,8-Difluoro-5-iodo-6-methoxymethoxy-2-pentylchroman

생성물 1

HCID 592152577,8-Difluoro-5-iodo-2-pentylchroman-6-ol

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 15413tert-Butyl methyl ether용매

실험 절차

9.2 ml of conc. HCl are added to a solution of 21.4 g (50.2 mmol) of 7,8-difluoro-5-iodo-6-methoxymethoxy-2-pentylchroman in 90 ml of THF, and the mixture is stirred at room temperature for 17 h. The batch is diluted with MTBE, and the solution is washed with water. The aqueous phase is extracted with MTBE, and the combined organic phases are washed with water and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The crude product is purified by column chromatography (SiO2, n-heptane:MTBE=1:1), giving 7,8-difluoro-5-iodo-2-pentylchroman-6-ol as a beige solid.

후처리

  1. washthe solution is washed with water
  2. extractionThe aqueous phase is extracted with MTBE
  3. washthe combined organic phases are washed with water and sat. sodium chloride soln
  4. customThe solution is dried
  5. concentrationconcentrated to dryness
  6. customThe crude product is purified by column chromatography (SiO2, n-heptane:MTBE=1:1)

출처 및 근거

ORD 기록
ord-8d6058bce2a94c9780855df87b4eda4d
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07678929B2

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