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Sodium Hydroxide → HCID 54499301, compound

HRID 436841
Notes
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Reaction equation

HRID 436841 reaction equation
[CH2:1]([NH2:7])[CH2:2][CH2:3][CH:4]=[CH:5][CH3:6].Br[CH2:9][CH:10]=[O:11].[OH-].[Na+]>CO>[CH2:1]([NH:7][CH2:9][CH:10]=[O:11])[CH2:2][CH2:3][CH:4]=[CH:5][CH3:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 14798Sodium HydroxideHCID 105131Acetaldehyde, bromo-HCID 533884Hex-4-enylamine

Product 1

HCID 54499301HCID 54499301, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Hex-4-enylamine (2.0 mole), the diethyl acetal of 2-bromoacetaldehyde (1.0 mole) and methanol (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux with stirring for a period of about 6 hours. After this time the reaction mixture is cooled to room temperature and sodium hydroxide (20 grams) is added. The reaction mixture is then stirred for an additional period of about 16 hours. The mixture is then filtered and the filtrate is distilled to yield the desired product the diethyl acetal of 2-hex-4-enylaminoacetaldehyde.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. customequipped with a mechanical stirrer
  2. temperaturethermometer and reflux condenser
  3. temperatureThe reaction mixture is heated
  4. temperatureat reflux
  5. stirringThe reaction mixture is then stirred for an additional period of about 16 hours
  6. filtrationThe mixture is then filtered
  7. distillationthe filtrate is distilled

Sources & evidence

ORD record
ord-1a6e4d97cb764b25807565169f36771a
Source dataset
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04028375

Reaction notes

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