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Ammonia → 10567-33-6

HRID 2398601
Notes
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Reaction equation

HRID 2398601 reaction equation
[ClH:1].[C:2]([CH2:6][CH2:7][C:8](=[NH:11])OC)([O:4][CH3:5])=[O:3].[NH3:12]>CO>[ClH:1].[C:2]([CH2:6][CH2:7][C:8]([NH2:11])=[NH:12])([O:4][CH3:5])=[O:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 222AmmoniaHCID 12300323Methyl 4-imino-4-methoxybutanoate hydrochloride

Product 1

HCID 1230032910567-33-6Yield 51.5%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a suspension of 16.5 g. (0.09 mole) of methyl β-carbomethoxypropionimidate hydrochloride in 20 ml. of methanol at ice bath temperatures is added 12 ml. of the same solvent containing 1.7 g. of dissolved ammonia gas. The reaction mixture is allowed to stir at room temperature for 2 hrs., followed by filtration of some insoluble material and concentration of the filtrate to near dryness. The residual white solids are treated with ethanol, filtered and dried, 7.8 g. (51.5% yield), m.p. 132° -134° C.

Workup

  1. additionTo a suspension of 16.5 g
  2. additionof the same solvent containing 1.7 g
  3. filtration, followed by filtration of some insoluble material and concentration of the filtrate
  4. additionThe residual white solids are treated with ethanol
  5. filtrationfiltered
  6. customdried

Sources & evidence

ORD record
ord-91a8ef7bd50140a2ab58e022e8cbe257
Source dataset
uspto-grants-1977_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04025504

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes