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Phenethyl bromide → 4-(2-Bromoethyl)benzaldehyde

HRID 892832
Notes
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Reaction equation

HRID 892832 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

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

Product 1

HCID 110851354-(2-Bromoethyl)benzaldehydeYield 40.8%

Reagents, catalysts & solvents 2

HCID 24193
Titanium Tetrachloride
Catalyst
HCID 6344DichloromethaneSolvent

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-2c700caf6ec74e62a32937116f8de256
Source dataset
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05120754

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes