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Aminoacetaldehyde dimethyl acetal → HCID 178495964, compound

HRID 1779916
Notes
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Reaction equation

HRID 1779916 reaction equation
[ClH:1].[S:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[CH2:7][C:8](=[NH:12])OCC.[CH3:13][O:14][CH:15]([O:18][CH3:19])[CH2:16][NH2:17]>O1CCCC1>[ClH:1].[CH3:13][O:14][CH:15]([O:18][CH3:19])[CH2:16][NH:17][C:8](=[NH:12])[CH2:7][C:3]1[S:2][CH:6]=[CH:5][CH:4]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 89728Aminoacetaldehyde dimethyl acetalHCID 19048678Ethyl 2-thiopheneethanimidate monohydrochloride

Product 1

HCID 178495964HCID 178495964, compoundYield 117.8%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

A mixture of ethyl 2-thiopheneethanimidate monohydrochloride (ester) (0.05 mol) in tetrahydrofuran (100 ml) was stirred under nitrogen. 2,2-dimethoxyethanamine (0.05 mol) was added portionwise upon cooling and the mixture was stirred overnight. The mixture was evaporated, yielding 15.6 g (100%) of N-(2,2-dimethoxyethyl)-2-thiopheneethanimidamide monohydrochloride (interm. 1).

Workup

  1. temperatureupon cooling
  2. stirringthe mixture was stirred overnight
  3. customThe mixture was evaporated

Sources & evidence

ORD record
ord-c50596464eb645bfb2eb263e8d736dbc
Source dataset
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05629308

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes