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Acetic Acid → Methyl 3-thiophenecarboximidate

HRID 1588569
Notes
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Reaction equation

HRID 1588569 reaction equation
[C:1]([C:3]1[CH:7]=[CH:6][S:5][CH:4]=1)#[N:2].C[O-].[Na+].[C:11](O)(=[O:13])C>CO>[S:5]1[CH:6]=[CH:7][C:3]([C:1](=[NH:2])[O:13][CH3:11])=[CH:4]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 176Acetic AcidHCID 74231Thiophene-3-carbonitrileHCID 10942334Sodium Methoxide

Product 1

HCID 15211507Methyl 3-thiophenecarboximidate

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

3-cyanothiophene (0.66 g, 6.0 mmol) was dissolved in methanol (6 ml), and sodium methoxide (0.03 g, 0.6 mmol) was added. The mixture was stirred at room temperature for 28 hours. After the reaction was completed, acetic acid (0.03 g, 0.6 mmol) was added to neutralize the reaction solution, and the solution was concentrated under reduced pressure. Diethyl ether (50 ml) was added to the concentrated residue, and insolubles were removed by filtration. The filtrate was concentrated under reduced pressure to give the crude product of methyl 3-thiophenecarboximidate.

Workup

  1. concentrationthe solution was concentrated under reduced pressure
  2. additionDiethyl ether (50 ml) was added to the concentrated residue, and insolubles
  3. customwere removed by filtration
  4. concentrationThe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-3590761d0ce24a0bbe455d7267adbb5a
Source dataset
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05223508

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes