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4-Iodo-3-methylbenzoic acid → (4-Iodo-3-methylphenyl)methanol

HRID 424800
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HRID 424800 반응식
[I:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[CH:4][C:3]=1[CH3:11]>C1COCC1>[I:1][C:2]1[CH:10]=[CH:9][C:5]([CH2:6][OH:7])=[CH:4][C:3]=1[CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 15173224-Iodo-3-methylbenzoic acid

생성물 1

HCID 53843601(4-Iodo-3-methylphenyl)methanol수율 95%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of 4-iodo-3-methyl-benzoic acid (5.2 g, 20 mmol) in THF (30 mL), is added 2.0 M borane-dimethyl sulfide complex in THF (40.0 mL, 80 mmol) dropwise. The reaction mixture is stirred overnight. The reaction mixture is quenched carefully at 0° C. with methanol (20 mL) and the mixture is evaporated to dryness under reduced pressure. The residue is partitioned between EtOAc (80 mL) and water (60 mL). The organic phase is washed with brine (60 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to a residue. The residue is purified by flash chromatography (AnaLogix, gradient EtOAc/Hexane) to give (4-Iodo-3-methyl-phenyl)-methanol as white solid (4.7 g, 95%). 1HNMR (CDCl3) (ppm): 2.4 (3H, s), 4.55 (2H, s), 6.8-7.75 (3H, m).

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customThe reaction mixture is quenched carefully at 0° C. with methanol (20 mL)
  2. customthe mixture is evaporated to dryness under reduced pressure
  3. customThe residue is partitioned between EtOAc (80 mL) and water (60 mL)
  4. washThe organic phase is washed with brine (60 mL)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure to a residue
  8. customThe residue is purified by flash chromatography (AnaLogix, gradient EtOAc/Hexane)

출처 및 근거

ORD 기록
ord-c972eae0d6c14fa291d1d2d6dbb11997
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106077B2

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