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Phenethyl bromide → 4-(2-Bromoethyl)benzaldehyde

HRID 892832
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HRID 892832 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

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

생성물 1

HCID 110851354-(2-Bromoethyl)benzaldehyde수율 40.8%

시약·촉매·용매 2

HCID 24193Titanium Tetrachloride촉매
HCID 6344
Dichloromethane
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-2c700caf6ec74e62a32937116f8de256
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05120754

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