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Acetonitrile → Acetic acid, azido-, ethyl ester

HRID 67700
Notes
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Reaction equation

HRID 67700 reaction equation
Cl[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].C(#N)C.[N-:11]=[N+:12]=[N-:13].[Na+]>O>[N:11]([CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4])=[N+:12]=[N-:13]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6342AcetonitrileHCID 7751Ethyl chloroacetateHCID 33557Sodium Azide

Product 1

HCID 69480Acetic acid, azido-, ethyl esterYield 76%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To a solution of 490 g. (4 moles) of ethyl chloroacetate in 1500 ml. of acetonitrile were added 260 g. (4 moles) of sodium azide, and the mixture was heated at the reflux temperature for 20 hours. After heating, the reaction mixture was poured into 1 liter of water with stirring for 1/2 hour. The organic phase was separated from the aqueous phase and evaporated in vacuo to dryness. The yellow residual oil was dissolved in 1200 ml. of diethyl ether and the solution was dried over magnesium sulfate. Evaporation of the diethyl ether in vacuo gave 391 g. (76% yield) of ethyl azidoacetate.

Workup

  1. temperatureAfter heating
  2. customThe organic phase was separated from the aqueous phase
  3. customevaporated in vacuo to dryness
  4. dissolutionThe yellow residual oil was dissolved in 1200 ml
  5. dry with materialof diethyl ether and the solution was dried over magnesium sulfate
  6. customEvaporation of the diethyl ether in vacuo
  7. customgave 391 g

Sources & evidence

ORD record
ord-2e24f4cc5a0741c6bf36e84fedfc7470
Source dataset
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04346076

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes