2-Methylpyridine 1-oxide → HCID 69592076, compound

HRID 965859Notes

Reaction equation

HRID 965859 reaction equation
[N+:1]1([O-:8])[C:2]([CH3:7])=[CH:3][CH:4]=[CH:5][CH:6]=1.C([O-])(C)(C)C.[K+].[Cl:15][C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][C:23]=1[Cl:24])[CH:19]=O>>[Cl:15][C:16]1[CH:17]=[C:18]([CH:19]=[CH:7][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][N+:1]=2[O-:8])[CH:21]=[CH:22][C:23]=1[Cl:24]

Participants

4

Reactant 3

HCID 136022-Methylpyridine 1-oxideHCID 227103,4-DichlorobenzaldehydeHCID 23665647Potassium tert-butoxide

Product 1

HCID 69592076HCID 69592076, compound

Procedure

Following the general method described in example 2a, 2-picoline-1-oxide was reacted with potassium tert.-butanolate and 3,4-dichloro-benzaldehyde. After extraction and chromatography the title compound was obtained as a yellow solid material. MS: m/e=265 (M+).

Workup

  1. extractionAfter extraction and chromatography the title compound
  2. customwas obtained as a yellow solid material

Sources & evidence

ORD record
ord-2e2a6cc872f147c3b68d19a389d80b2c
Source dataset
uspto-grants-2005_10
Patent number
US06951875B2

Reaction notes

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