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Dichloromethane → HCID 68670764, compound

HRID 2070944
Notes
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Reaction equation

HRID 2070944 reaction equation
O[CH2:2][C:3]1[CH:4]=[C:5]([C:11](O)([CH3:13])[CH3:12])[C:6]([CH3:10])=[N:7][C:8]=1[CH3:9].C(Cl)[Cl:16]>>[Cl:16][CH2:2][C:3]1[C:8]([CH3:9])=[N:7][C:6]([CH3:10])=[C:5]([C:11]([CH3:13])=[CH2:12])[CH:4]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6344DichloromethaneHCID 68670777HCID 68670777, compound

Product 1

HCID 68670764HCID 68670764, compound

Procedure

To a stirring solution of 2-(5-(hydroxymethyl)-2,6-dimethylpyridin-3-yl)propan-2-ol in 10 mL of CH2Cl2 was added 1.5 mL of SO2Cl2. After 11 h at r.t., the solution was concentrated and CH2Cl2 and 10 mL of sat. NaHCO3 solution were added, and the layers were separated. The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated. Purification by flash silica gel chromatography (20% Et2O/hexanes) provided 96.5 mg of the desired 3-(chloromethyl)-2,6-dimethyl-5-(prop-1-en-2-yl)pyridine as a mixture.

Workup

  1. concentrationthe solution was concentrated
  2. additionCH2Cl2 and 10 mL of sat. NaHCO3 solution were added
  3. customthe layers were separated
  4. washThe organic layer was washed with brine
  5. dry with material
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
dried over Na2SO4
  • filtrationfiltered
  • concentrationconcentrated
  • customPurification by flash silica gel chromatography (20% Et2O/hexanes)
  • Sources & evidence

    ORD record
    ord-74c2ebecbf054444940569c65eedfc13
    Source dataset
    uspto-grants-2012_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08299267B2

    Reaction notes

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