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1,3-Propanediol → 2-(4-Bromo-3-fluorophenyl)-1,3-dioxane

HRID 1177388
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HRID 1177388 반응식
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][C:3]=1[F:10].[CH2:11](O)[CH2:12][CH2:13][OH:14].O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]2[O:14][CH2:13][CH2:12][CH2:11][O:7]2)=[CH:4][C:3]=1[F:10]
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참가 물질

5

반응물 3

HCID 104421,3-PropanediolHCID 521998p-Toluenesulfonic acid monohydrateHCID 27834114-Bromo-3-fluorobenzaldehyde

생성물 1

HCID 671119942-(4-Bromo-3-fluorophenyl)-1,3-dioxane

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

4-Bromo-3-fluorobenzaldehyde (100.00 g, 492.6 mmol) was added to toluene (1 L). Propane-1,3-diol (42.72 mL, 591.1 mmol), and p-toluenesulfonic acid monohydrate (4.685 g, 24.63 mmol) were added to above and the reaction mixture was brought to reflux. The solvent (500 mL) was azeotroped off using a dean stark trap. The reaction mixture was cooled and extracted with sat. aqueous sodium bicarbonate (500 mL). The organics were dried over magnesium sulfate and concentrated in vacuo to give 2-(4-bromo-3-fluorophenyl)-1,3-dioxane as a white solid. MS (ESI) m/z: Calculated: 260.0/262.0; Observed: 260.9 (M++1).

후처리

  1. temperatureto reflux
  2. customThe solvent (500 mL) was azeotroped off
  3. temperatureThe reaction mixture was cooled
  4. extractionextracted with sat. aqueous sodium bicarbonate (500 mL)
  5. dry with materialThe organics were dried over magnesium sulfate
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-10ed149607a74ddca645e0b4687e5c6c
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07842685B2

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