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Thionyl Chloride → HCID 22938820, compound

HRID 856717
Notes
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Reaction equation

HRID 856717 reaction equation
O[CH2:2][C:3]1[CH:7]=[N:6][N:5]([CH2:8][CH2:9][CH3:10])[N:4]=1.S(Cl)([Cl:13])=O>>[Cl:13][CH2:2][C:3]1[CH:7]=[N:6][N:5]([CH2:8][CH2:9][CH3:10])[N:4]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24386Thionyl ChlorideHCID 22938707HCID 22938707, compound

Product 1

HCID 22938820HCID 22938820, compound

Procedure

To a solution of aluminum lithium hydride (1.57 g) in THF (140 ml) was added dropwise methyl 2-propyl-1,2,3-triazole-4-carboxylate (7.0 g) in. THF (70 ml) at 0° C. The mixture was stirred for 1 hour at room temperature, and an aqueous solution of saturated sodium thiosulfate was added to the mixture at 0° C. The mixture was filtered with Celite, and washed with ethanol. The solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, to give 4-hydroxymethyl-2-propyl-1,2,3-triazole (5.9 g). To 4-hydroxymethyl-2-propyl-1,2,3-triazole (4.0 g), thionyl chloride (32 ml) was added to the mixture at 0° C., and the mixture was heated to reflux for 1 hour. After allowing the mixture to be cooled to room temperature, the solvent was removed under reduced pressure, to give 4-chloromethyl-2-propyl-1,2,3-triazole (4.2 g).

Workup

  1. temperature
the mixture was heated
  • temperatureto reflux for 1 hour
  • customthe solvent was removed under reduced pressure
  • Sources & evidence

    ORD record
    ord-b411308f720e4b9abf089a315746515e
    Source dataset
    uspto-grants-2007_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07262185B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes