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Water → Pyridine-4-carboxaldehyde (3-Chloropropyl)imine

HRID 1740568
Notes
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Reaction equation

HRID 1740568 reaction equation
Cl.[Cl:2][CH2:3][CH2:4][CH2:5][NH2:6].O.[N:8]1[CH:13]=[CH:12][C:11]([CH:14]=O)=[CH:10][CH:9]=1.C([O-])([O-])=O.[K+].[K+]>C(Cl)Cl>[Cl:2][CH2:3][CH2:4][CH2:5][N:6]=[CH:14][C:11]1[CH:12]=[CH:13][N:8]=[CH:9][CH:10]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 133894-PyridinecarboxaldehydeHCID 114690951-Propanamine, 3-chloro-, hydrochloride

Product 1

HCID 10655047Pyridine-4-carboxaldehyde (3-Chloropropyl)imine

Reagents, catalysts & solvents 1

HCID 6344
Dichloromethane
Solvent

Procedure

To 3-chloropropylamine HCl (15.1 g, 0.120 moles (hereinafter mol)) and H2O (100 mL) was added pyridine-4-carboxaldehyde (9.55 mL, 0.100 mol), then K2CO3 (8.28 g, 0.060 mol) then CH2Cl2 (100 mL) and the mixture was stirred for 40 min. The phases were separated and the aq phase was extracted with additional CH2Cl2 (2×50 mL), dried (Na2SO4) and concentrated to afford 17.1 g (94%) 1H NMR (CD3Cl): d 8.69 (d, J=4.5 Hz, 2H, 8.32 (s, 1H), 8.28 (s, 1H), 7.58 (d, J=4.5 Hz, 2H), 3.71 (m, 2H), 3.63 (t, J=6 Hz, 2H), 2.24 (t, J=6Hz, 2H). The presence of 9% of the aldehyde was evident by 1H NMR.

Workup

  1. customThe phases were separated
  2. extractionthe aq phase was extracted with additional CH2Cl2 (2×50 mL)
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated
  5. customto afford 17.1 g (94%) 1H NMR (CD3Cl): d 8.69 (

Sources & evidence

ORD record
ord-ac26d30ebb8840d1a6f370d9f234922c
Source dataset
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05969184

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes