2-Chloroethanol → Ethyl 2-(2-chloroethoxy)acetate

HRID 2210821Notes

Reaction equation

HRID 2210821 reaction equation
[H-].[Na+].[Cl:3][CH2:4][CH2:5][OH:6].Br[CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10]>CN(C)C=O>[Cl:3][CH2:4][CH2:5][O:6][CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10]

Participants

5

Procedure

A suspension of 25.0 g of sodium hydride (as a 60 % w/w suspension in mineral oil) in 100 ml of dimethylformamide was added dropwise to a solution of 50 g of 2-chloroethanol and 104 g of ethyl bromoacetate in 350 m of dimethylformamide at between -45° C. and -40° C., and the mixture was stirred at the same temperature for 1 hour, at between -30° C. and -25° C. for 2 hours, at -5° C. -5° C. for hour and then at room temperature for 2 hours. At the end of this time, it was concentrated by evaporation under reduced pressure, and 1000 ml of toluene were added to the residue. The solution was then washed with water, and the solvent was removed by evaporation under reduced pressure. Distillation gave 77.6 g (yield 75%) of the title compound, boiling at 57°-58° C./2.5 mmHg (333 Pa).

Workup

  1. waitat room temperature for 2 hours
  2. concentrationAt the end of this time, it was concentrated by evaporation under reduced pressure, and 1000 ml of toluene
  3. additionwere added to the residue
  4. washThe solution was then washed with water
  5. customthe solvent was removed by evaporation under reduced pressure
  6. distillationDistillation

Sources & evidence

ORD record
ord-d7158dfef9fb46e3b0bba8dcaec13175
Source dataset
uspto-grants-1995_10
Patent number
US05461051

Reaction notes

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