Sodium Carbonate → 2-Chloro-4-pyridinecarboxaldehyde

HRID 362618

反応式

HRID 362618 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([CH2:8][OH:9])[CH:5]=[CH:4][N:3]=1.C1C(=O)N(Br)C(=O)C1.C([O-])([O-])=O.[K+].[K+].C([O-])([O-])=O.[Na+].[Na+]>CCOC(C)=O>[Cl:1][C:2]1[CH:7]=[C:6]([CH:8]=[O:9])[CH:5]=[CH:4][N:3]=1

参加物

6

反応物 4

HCID 10340Sodium CarbonateHCID 11430Potassium CarbonateHCID 67184N-bromobutanimide2 回HCID 7062237(2-Chloropyridin-4-yl)methanol

生成物 1

HCID 27629942-Chloro-4-pyridinecarboxaldehyde

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

A suspension of 2-chloro-4-pyridinemethanol (8.0 g, 55.9 mmol), NBS (14.9 g, 83.9 mmol), and K2CO3 (11.75 g, 97.1 mmol) in EtOAc was refluxed for 3 h. A second portion of NBS (14.9 g, 83.9 mmol) and Na2CO3 (12.0 g, 114 mmol) were added and the reaction was heated to reflux for an additional 3.5 h, cooled and filtered through a pad of celite. The filtrate, after concentrattion to a small volume, was subjected to flash chromatography eluting with 0.5-4% CH3OH/CH2Cl2. The fractions containing product were combined, washed successively with sat aq NaHCO3, 10% Na2S2O3, and brine, dried (MgSO4) and concentrated in vacuo to give the title compound as a light yellow solid; yield 5.3 g (67%). 1H NMR (CDCl3) δ10.06 (s, 1H), 8.66 (d, 1H, J=5.0 Hz), 7.76 (s, 1H), 7.66 (d, 1H, J=5.0 Hz).

後処理

  1. temperaturewas refluxed for 3 h
  2. temperaturethe reaction was heated
  3. temperatureto reflux for an additional 3.5 h
  4. temperaturecooled
  5. filtrationfiltered through a pad of celite
  6. washeluting with 0.5-4% CH3OH/CH2Cl2
  7. additionThe fractions containing product
  8. washwashed successively with sat aq NaHCO3, 10% Na2S2O3, and brine
  9. dry with materialdried (MgSO4)
  10. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-20c0eae67f40479784f43ae9df7def72
出典データセット
uspto-grants-1999_02
特許番号
US05869660

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