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

HRID 1177388
ノート
印刷プレビュー

反応式

HRID 1177388 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-10ed149607a74ddca645e0b4687e5c6c
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07842685B2

反応ノート

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