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Nitromethane → (E)-2-cyclopropyl-3-(2-nitrovinyl)-6-(trifluoromethyl)pyridine

HRID 1626524
Notes
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Reaction equation

HRID 1626524 reaction equation
[CH:1]1([C:4]2[N:11]=[C:10]([C:12]([F:15])([F:14])[F:13])[CH:9]=[CH:8][C:5]=2[CH:6]=O)[CH2:3][CH2:2]1.[N+:16]([CH3:19])([O-:18])=[O:17].Cl.CN.C([O-])(=O)C.[Na+]>>[CH:1]1([C:4]2[C:5](/[CH:6]=[CH:19]/[N+:16]([O-:18])=[O:17])=[CH:8][CH:9]=[C:10]([C:12]([F:15])([F:14])[F:13])[N:11]=2)[CH2:3][CH2:2]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 6375NitromethaneHCID 517045Sodium AcetateHCID 6364545Methylamine hydrochlorideHCID 866644002-Cyclopropyl-6-(trifluoromethyl)nicotinaldehyde

Product 1

HCID 67287702(E)-2-cyclopropyl-3-(2-nitrovinyl)-6-(trifluoromethyl)pyridineYield 16.7%

Procedure

2-Cyclopropyl-6-(trifluoromethyl)nicotinaldehyde (130 mg, 0.604 mmol) was diluted with nitromethane (229 μL, 4.23 mmol) followed by the addition of methylamine hydrochloride (24.5 mg, 0.363 mmol) and sodium acetate (29.7 mg, 0.363 mmol). After stirring for 4 hours, the reaction was loaded onto silica gel and eluted with 5% ethyl acetate/hexanes to 50% ethyl acetate/hexanes to yield (E)-2-cyclopropyl-3-(2-nitrovinyl)-6-(trifluoromethyl)pyridine (26 mg, 0.101 mmol, 16.7% yield).

Workup

  1. washeluted with 5% ethyl acetate/hexanes to 50% ethyl acetate/hexanes

Sources & evidence

ORD record
ord-ea5c0ceb205f4efeacc5e383cd75a10e
Source dataset
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08785445B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes