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Ammonium Chloride → HCID 66777829, compound

HRID 2091308
Notes
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Reaction equation

HRID 2091308 reaction equation
[CH3:1][C:2]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[S:4][C:3]=1[CH:11]=[O:12].[CH:13]1([Mg]Br)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.[Cl-].[NH4+].C[N+]1([O-])CCOCC1>O1CCCC1.[Ru]([O-])(=O)(=O)=O.C([N+](CCC)(CCC)CCC)CC.C(#N)C>[CH:13]1([C:11]([C:3]2[S:4][C:5]3=[N:6][CH:7]=[CH:8][CH:9]=[C:10]3[C:2]=2[CH3:1])=[O:12])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 25517Ammonium ChlorideHCID 82029Methyl morpholine oxideHCID 82374291HCID 82374291, compoundHCID 178419651HCID 178419651, compound

Product 1

HCID 66777829HCID 66777829, compoundYield 85%

Reagents, catalysts & solvents 3

HCID 178419074
HCID 178419074, compound
Catalyst
HCID 6342AcetonitrileSolvent
HCID 8028TetrahydrofuranSolvent2×

Procedure

To a solution (60 mL) of 3-methylthieno[2,3-b]pyridine-2-carbaldehyde (2.07 g) synthesized above in tetrahydrofuran was added a 1.0M solution (17.6 mL) of cyclohexylmagnesium bromide in tetrahydrofuran at 0° C., and the mixture was stirred for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (10-50% ethyl acetate/hexane) to give a yellow solid. To a mixture of the obtained solid, 4-methylmorpholine N-oxide (1.81 g) and acetonitrile (40 mL) was added tetrapropylammonium perruthenate (238 mg), and the mixture was stirred at room temperature for 3 hr, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (0-30% ethyl acetate/hexane) to give the title object compound (1.50 g, 85%) as a white solid.

Workup

  1. customto quench
  2. customthe reaction
  3. extractionthe reaction mixture was extracted with ethyl acetate
  4. washThe extract was washed with saturated brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (10-50% ethyl acetate/hexane)
  8. customto give a yellow solid
  9. stirringthe mixture was stirred at room temperature for 3 hr
  10. concentrationconcentrated under reduced pressure
  11. customThe residue was purified by silica gel column chromatography (0-30% ethyl acetate/hexane)

Sources & evidence

ORD record
ord-d28ca41f5eff4e97aeb2cecf3550d2f2
Source dataset
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08436043B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes