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Iodoethane → 4-(1-Ethyl-4-piperidinyl)-1-butanol

HRID 1044863
Notes
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Reaction equation

HRID 1044863 reaction equation
Cl.[NH:2]1[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9][CH2:10][CH2:11][OH:12])[CH2:4][CH2:3]1.C(=O)([O-])[O-].[K+].[K+].I[CH2:20][CH3:21]>C(#N)C>[CH2:20]([N:2]1[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9][CH2:10][CH2:11][OH:12])[CH2:4][CH2:3]1)[CH3:21]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 27846674-(4-Piperidyl)-1-butanol hydrochloride

Product 1

HCID 583060664-(1-Ethyl-4-piperidinyl)-1-butanolYield 55.9%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

To stirring solution of 4-(4-piperidinyl)-1-butanol hydrochloride (4.51 g, 23.28 mmol) and potassium carbonate (8.04 g, 58.2 mmol) in dry acetonitrile (60 ml) was added iodoethane (2.070 ml, 25.6 mmol). The reaction mixture was allowed to stir at room temperature for 4 hours. The reaction mixture was concentrated in vacuo and the residue partitioned between water (20 ml) and ethyl acetate (30 ml). The aqueous was re-extracted with ethyl acetate (1×30 ml) then dichloromethane (1×30 ml), the organic layers dried by passage through a hydrophobic frit), combined and concentrated in vacuo to give the title compound as a yellow gum (2.41 g).

Workup

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customthe residue partitioned between water (20 ml) and ethyl acetate (30 ml)
  3. extractionThe aqueous was re-extracted with ethyl acetate (1×30 ml)
  4. dry with materialdichloromethane (1×30 ml), the organic layers dried by passage through a hydrophobic frit),
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-4dfcc2c2b8a44f54b4cde0af5f947f7c
Source dataset
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08563717B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes