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Propanal → p-Azido-2-methylcinnamaldehyde

HRID 1885047
Notes
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Reaction equation

HRID 1885047 reaction equation
[N:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1)=[N+:2]=[N-:3].[CH:12](=[O:15])[CH2:13]C.[OH-].[Na+].[CH:18](O)(C)C>O>[N:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=[CH:13][CH:12]=[O:15])=[C:6]([CH3:18])[CH:5]=1)=[N+:2]=[N-:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 527Propanal2×HCID 3776IsopropanolHCID 14798Sodium HydroxideHCID 903854-Azidobenzaldehyde

Product 1

HCID 86589921p-Azido-2-methylcinnamaldehydeYield 62%

Reagents, catalysts & solvents 1

HCID 962Water
Solvent
2×

Procedure

4-Azidobenzaldehyde (29.42 g, 0.2 mol) and propionaldehyde (12.22 g, 0.2 mol) were dissolved in a solvent mixture of isopropyl alcohol (100 g) and pure water (50 g). Under cooling in an ice bath, sodium hydroxide (2 g) dissolved in pure water (20 g) was added to the solution, and the mixture was stirred for two hours. Propionaldehyde (12.22 g, 0.2 mol) was added again to the mixture, and the resultant mixture was stirred for a further three hours. The formed precipitates were collected through filtration and dried, to thereby yield 23.14 g of p-azido-2-methylcinnamaldehyde as yellow crystals (yield: 62%). The compound thus obtained was identified on the basis of the 1H-NMR measurements shown in Table 1.

Workup

  1. temperatureUnder cooling in an ice bath
  2. additionwas added to the solution
  3. customThe formed precipitates
  4. filtrationwere collected through filtration
  5. customdried

Sources & evidence

ORD record
ord-cba7d836589841a992d0f75199a96b65
Source dataset
uspto-grants-2004_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06768027B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes