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Potassium Carbonate → 4-(4-BROMOPHENYL)-2-BUTANONE

HRID 549364
ノート
印刷プレビュー

反応式

HRID 549364 の反応式
[CH3:1][C:2](=[O:7])[CH2:3][C:4](=O)[CH3:5].[Br:8][C:9]1[CH:16]=[CH:15]C(CBr)=[CH:11][CH:10]=1.C(=O)([O-])[O-].[K+].[K+]>CO>[Br:8][C:9]1[CH:16]=[CH:15][C:5]([CH2:4][CH2:3][C:2](=[O:7])[CH3:1])=[CH:11][CH:10]=1
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 11430Potassium CarbonateHCID 31261AcetylacetoneHCID 685274-Bromobenzyl bromide

生成物 1

HCID 10515164-(4-BROMOPHENYL)-2-BUTANONE収率 67%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A mixture of 2,4-pentanedione (200 mg, 206 μL, 2 mmol), the 4-bromobenzyl bromide (2 mmol), and anhydrous potassium carbonate (276 mg, 2 mmol) in methanol (10 mL) was heated at reflux temperature for 16 h. The mixture was then cooled to room temperature, methanol was removed under reduced pressure, and the resulting residue was partitioned between ethyl acetate (10 mL) and water (10 mL). The organic layer was separated, and the aqueous layer was extracted further with ethyl acetate (3×10 mL). The combined organic phase was washed with water (10 mL), dried over anhydrous Na2SO4, and then the solvent was removed under pressure. The resulting oil was chromatographed on a silica gel column using hexanes-ethyl acetate as mobile phase to give 4-(4-bromophenyl)-2-butanone as a clear liquid (302 mg, 67%): Rf=0.38 (hexanes-ethyl acetate 3:1 v/v); 1H NMR (400 MHz, CDCl3): δ 2.15 (s, 3H), 2.75 (t, J=7.2 Hz, 2H), 2.86 (t, J=7.2 Hz, 2H), 7.07 (d, J=8 Hz, 2H), 7.40 (d, J=8.4 Hz, 21; 13C NMR (100 MHz, CDCl3): δ 29.2, 30.2, 44.9, 120.0, 130.2, 131.7, 140.2, 207.4; HRMS (ESI) Calcd. for C10H11BrONa: 248.9891 [M+Na+]. Found: 248.9880.

後処理

  1. temperatureat reflux temperature for 16 h
  2. custommethanol was removed under reduced pressure
  3. customthe resulting residue was partitioned between ethyl acetate (10 mL) and water (10 mL)
  4. customThe organic layer was separated
  5. extractionthe aqueous layer was extracted further with ethyl acetate (3×10 mL)
  6. washThe combined organic phase was washed with water (10 mL)
  7. dry with materialdried over anhydrous Na2SO4
  8. customthe solvent was removed under pressure
  9. customThe resulting oil was chromatographed on a silica gel column

出典と根拠

ORDレコード
ord-d3658ac7205542eba4e2d16ef5a94d74
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07943650B2

反応ノート

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