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Dimethyl Sulfoxide → 4-Bromo-3'-methoxybenzophenone

HRID 1633543
ノート
印刷プレビュー

反応式

HRID 1633543 の反応式
CS(C)=O.FC(F)(F)C(O)=O.[Br:12][C:13]1[CH:18]=[CH:17][C:16]([CH:19]([C:21]2[CH:26]=[CH:25][CH:24]=[C:23]([O:27][CH3:28])[CH:22]=2)[OH:20])=[CH:15][CH:14]=1.CCN(CC)CC>C(Cl)Cl>[Br:12][C:13]1[CH:14]=[CH:15][C:16]([C:19]([C:21]2[CH:26]=[CH:25][CH:24]=[C:23]([O:27][CH3:28])[CH:22]=2)=[O:20])=[CH:17][CH:18]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 679Dimethyl SulfoxideHCID 6422Trifluoroacetic acidHCID 8471TriethylamineHCID 18507125HCID 18507125、化合物

生成物 1

HCID 27570324-Bromo-3'-methoxybenzophenone

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒3 回

実験手順

To a solution of DMSO (8.13 mL, 114.7 mmol) in CH2Cl2 (80 mL) at −78 was added solution of trifluoroacetic acid (TFAA) (12.12 mL, 86.0 mmol) in CH2Cl2 (50 mL) over 5 min. The mixture was stirred for 20 min and a solution of (4-bromo-phenyl)-(3-methoxy-phenyl)-methanol (16.8 g, 57.4 mmol) in CH2Cl2 (50 mL) was added dropwise over 5 min. The reaction mixture was stirred at −78° C. for 30 min and Et3N (24.0 mL, 172 mmo) was added. The mixture was stirred at −78° C. for an additional 30 min and at room temperature for 1 h. The CH2Cl2 layer was washed with brine (3×30 mL), dried over Na2SO4 and concentrated. Purification with hexanes/EtOAc (10:1) afforded 16.0 9 of (4-Bromo-phenyl)-(3-methoxy-phenyl)-methanone. 1HNMR (400 MHz, CDCl3) δ 7.67-7.66 (comp, 2H), 7.64-7.60 (comp, 2H), 7.37 (m, 1H), 7.34-7.27 (comp, 2H), 7.14-7.11 (m, 1H), 3.84 (s, 3H).

後処理

  1. stirringThe reaction mixture was stirred at −78° C. for 30 min
  2. stirringThe mixture was stirred at −78° C. for an additional 30 min and at room temperature for 1 h
  3. washThe CH2Cl2 layer was washed with brine (3×30 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated
  6. customPurification with hexanes/EtOAc (10:1)

出典と根拠

ORDレコード
ord-b048b65f4a0e4aa2b7f23043002f87ff
出典データセット
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06503905B1

反応ノート

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