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Thionyl Chloride → (2-Iodo-3-methylphenyl)methanol

HRID 723182
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HRID 723182 반응식
S(Cl)(Cl)=O.[I:5][C:6]1[C:14]([CH3:15])=[CH:13][CH:12]=[CH:11][C:7]=1[C:8](O)=[O:9]>>[I:5][C:6]1[C:14]([CH3:15])=[CH:13][CH:12]=[CH:11][C:7]=1[CH2:8][OH:9]
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참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 27593652-Iodo-3-methylbenzoic acid

생성물 1

HCID 15717698(2-Iodo-3-methylphenyl)methanol수율 26.4%

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온도
50 °C

실험 절차

Thionyl chloride [5 mL] was added to 2-iodo-3-methyl-benzoic acid (2.00 g, 7.63 mmol) at room temperature and heated to 50° C. for 1 hour. The solution was then cooled and evaporated. The crude residue was dissolved in ethyl acetate, washed with brine and dried with magnesium sulfate. The crude product was then dissolved in THF [5 mL] and a 1M solution of lithium aluminum hydride [10.7 mL] was added at room temperature and stirred for 1 hour. Water [0.1 mL] and 15% NaOH [0.1 mL] were added followed by evaporation. Column chromatography (50% EtOAc in hexanes) of the residue yielded the title compound (0.50 g, 26%) as a solid. 1H-NMR (CDCl3): δ 3.20 (t, 2H, J=7.6 Hz), 2.98 (s, 3H), 2.52 (t, 2H, J=7.2 Hz), 2.09 (m, 2H).

후처리

  1. temperatureThe solution was then cooled
  2. customevaporated
  3. dissolutionThe crude residue was dissolved in ethyl acetate
  4. washwashed with brine
  5. dry with materialdried with magnesium sulfate
  6. dissolutionThe crude product was then dissolved in THF [5 mL]
  7. additiona 1M solution of lithium aluminum hydride [10.7 mL] was added at room temperature
  8. additionWater [0.1 mL] and 15% NaOH [0.1 mL] were added
  9. customfollowed by evaporation

출처 및 근거

ORD 기록
ord-034d67d5167c4a4ab724b7739680538f
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07138530B2

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