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Potassium Phosphate, Tribasic → 5-Bromo-2-cyclopropylbenzaldehyde

HRID 537685
ノート
印刷プレビュー

反応式

HRID 537685 の反応式
[O-]P([O-])([O-])=O.[K+].[K+].[K+].Br[C:10]1[CH:17]=[CH:16][C:15]([Br:18])=[CH:14][C:11]=1[CH:12]=[O:13].[CH:19]1(B(O)O)[CH2:21][CH2:20]1>N#N.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Br:18][C:15]1[CH:16]=[CH:17][C:10]([CH:19]2[CH2:21][CH2:20]2)=[C:11]([CH:14]=1)[CH:12]=[O:13]
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 62657Potassium Phosphate, TribasicHCID 2760897Cyclopropylboronic acidHCID 135400692,5-Dibromobenzaldehyde

生成物 1

HCID 580613585-Bromo-2-cyclopropylbenzaldehyde

試薬・触媒・溶媒 1

HCID 178514306HCID 178514306、化合物触媒

実験手順

To a mixed solution of toluene (2250 ml) and distilled water (250 ml) at 0° C. is added finely ground potassium phosphate tribasic (699.23 g, 3.29 mol) portionwise over 10 minutes. This mixture is then allowed to warm to room temperature, followed by the addition of 2,5-dibromobenzaldehyde (235.0 g, 890 mmol) and cyclopropylboronic acid (68.92 g, 801 mmol). After stirring at room temperature for 50 minutes under a blanket of nitrogen tetrakis(triphenylphosphine)palladium (102.89 g, 89 mmol) is added over 10 minutes, washing residual solid with toluene (50 ml). The reaction mixture is then stirred at 80° C. for 22 hours, followed by cooling to room temperature and addition of distilled water (500 ml). The mixture is filtered through a pad of silica (washing with additional ethyl acetate) and the aqueous phase is extracted with ethyl acetate (2×300 ml). The combined organic extracts are washed with brine (500 ml), dried with anhydrous magnesium sulfate and concentrated under reduced pressure. The residue is purified by chromatography on silica gel (iso-hexane/ethyl acetate as eluant) followed by distillation under reduced pressure to afford 5-bromo-2-cyclopropylbenzaldehyde as a yellow oil.

後処理

  1. distillationTo a mixed solution of toluene (2250 ml) and distilled water (250 ml) at 0° C.
  2. additionis added over 10 minutes
  3. washwashing residual solid with toluene (50 ml)
  4. temperatureby cooling to room temperature
  5. additionaddition of distilled water (500 ml)
  6. filtrationThe mixture is filtered through a pad of silica (washing with additional ethyl acetate)
  7. extractionthe aqueous phase is extracted with ethyl acetate (2×300 ml)
  8. washThe combined organic extracts are washed with brine (500 ml)
  9. dry with materialdried with anhydrous magnesium sulfate
  10. concentrationconcentrated under reduced pressure
  11. customThe residue is purified by chromatography on silica gel (iso-hexane/ethyl acetate as eluant)
  12. distillationfollowed by distillation under reduced pressure

出典と根拠

ORDレコード
ord-2993530493a14e5b9999b381f6dd1ac7
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08865623B2

反応ノート

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