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Sodium Iodide → Methyl(2-(piperidin-1-yl)ethyl)amine

HRID 34712
Notes
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Reaction equation

HRID 34712 reaction equation
Cl.Cl[CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1.[I-].[Na+].[CH3:13][NH2:14]>CO>[CH3:13][NH:14][CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 5238Sodium IodideHCID 6329MethylamineHCID 74826Piperidine, 1-(2-chloroethyl)-, hydrochloride

Product 1

HCID 3157473Methyl(2-(piperidin-1-yl)ethyl)amineYield 73%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A solution of 8.0 g of N-(2-chloroethyl)piperidine hydrochloride and 0.5 g of sodium iodide in 60 ml of methanol which contained 40% of methylamine was reacted at 70° C. in a sealed tube for 20 hours. After allowing the reaction mixture to cool down, the reaction mixture was concentrated under reduced pressure. The residue was added with ether, followed by a further addition of 10 g of ground sodium hydroxide. The resulting mixture was stirred for 2 hours. The insoluble material was filtered off and the filtrate was concentrated under the atmospheric pressure. The residue was distilled under reduced pressure to give 4.5 g of a fraction at 80° C./18 Torr (yield: 73%).

Workup

  1. customwas reacted at 70° C. in a sealed tube for 20 hours
  2. temperatureto cool down
  3. concentrationthe reaction mixture was concentrated under reduced pressure
  4. additionThe residue was added with ether
  5. additionfollowed by a further addition of 10 g of ground sodium hydroxide
  6. filtrationThe insoluble material was filtered off
  7. concentrationthe filtrate was concentrated under the atmospheric pressure
  8. distillationThe residue was distilled under reduced pressure
  9. customto give 4.5 g of a fraction at 80° C./18 Torr (yield: 73%)

Sources & evidence

ORD record
ord-50a24f73a84448bdaee945495527e333
Source dataset
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04762927

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes