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Phenethyl bromide → 4-(2-Bromoethyl)benzaldehyde

HRID 892832
ノート
印刷プレビュー

反応式

HRID 892832 の反応式
[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:10][O:11]C(Cl)Cl.C([O-])(O)=O.[Na+].C(OCC)(=O)C>C(Cl)Cl.[Ti](Cl)(Cl)(Cl)Cl>[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([CH:10]=[O:11])=[CH:6][CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 7666Phenethyl bromideHCID 8857Ethyl AcetateHCID 21004Methane, dichloromethoxy-HCID 516892Sodium Bicarbonate

生成物 1

HCID 110851354-(2-Bromoethyl)benzaldehyde収率 40.8%

試薬・触媒・溶媒 2

HCID 24193Titanium Tetrachloride触媒
HCID 6344
Dichloromethane
溶媒

実験手順

To a solution of (2-bromoethyl)benzene (100 mmol, 18.5 g) in methylene chloride (185 ml) at 0° C. was added dropwise titanium tetrachloride (200 mmol, 22 ml). The mixture was stirred for 10 minutes and alpha,alpha-dichloromethyl methyl ether (100 mmol, 9 ml) was added dropwise. The reaction mixture was stirred at room temperature for 1 hour and poured into saturated NaHCO3 (1 liter). Ethyl acetate (750 ml) was added and the solution was filtered through diatomaceous earth, the organic layer separated, dried (Na2SO4) and solvent removed in vacuo. The residue was triturated with hexane to afford 8.7 g of title product; m.p. 49°-52° C.

後処理

  1. stirringThe reaction mixture was stirred at room temperature for 1 hour
  2. filtrationthe solution was filtered through diatomaceous earth
  3. customthe organic layer separated
  4. dry with materialdried (Na2SO4) and solvent
  5. customremoved in vacuo
  6. customThe residue was triturated with hexane

出典と根拠

ORDレコード
ord-2c700caf6ec74e62a32937116f8de256
出典データセット
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05120754

反応ノート

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