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Ethyl bromoacetate → Ethyl 2-(propylamino)acetate

HRID 1980845
Notes
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Reaction equation

HRID 1980845 reaction equation
Br[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].[CH2:8]([NH2:11])[CH2:9][CH3:10]>C(Cl)Cl>[CH2:8]([NH:11][CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4])[CH2:9][CH3:10]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 7748Ethyl bromoacetateHCID 7852Propylamine

Product 1

HCID 13454968Ethyl 2-(propylamino)acetate

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

5.53 ml (50 mM) of ethyl bromoacetate were added dropwise to a solution of 20.5 ml (250 mM) of n-propylamine in 50 ml of CH2Cl2 at 0°. The reaction mixture was then warmed to room temperature and stirred for 1 hour, then concentrated to remove volatiles through a short path distillation head at atmospheric pressure. The residual liquid was taken up in ether and washed with saturated aqueous NaHCO3. The layers were separated and the ether layer was washed once with brine then dried over anhydrous MgSO4. The ether was removed to yield 7.16 g of ethyl N-(n-propyl)-glycinate as a pale yellow liquid.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. concentrationconcentrated
  2. customto remove volatiles
  3. distillationthrough a short path distillation head at atmospheric pressure
  4. washwashed with saturated aqueous NaHCO3
  5. customThe layers were separated
  6. washthe ether layer was washed once with brine
  7. dry with materialthen dried over anhydrous MgSO4
  8. customThe ether was removed

Sources & evidence

ORD record
ord-f7bf8b12e954401e8e8fec13146f5f70
Source dataset
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04511568

Reaction notes

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