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Acetone → 5-Chloro-6-(hydroxymethyl)-3-pyridinecarbaldehyde

HRID 420728
ノート
印刷プレビュー

反応式

HRID 420728 の反応式
C(O)(=O)C(O)=O.[Cl:7][C:8]1[C:9]([CH2:19][OH:20])=[N:10][CH:11]=[C:12]([CH:14]2OCC[O:15]2)[CH:13]=1.CC(C)=O.[OH-].[Na+]>O>[Cl:7][C:8]1[CH:13]=[C:12]([CH:14]=[O:15])[CH:11]=[N:10][C:9]=1[CH2:19][OH:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 180AcetoneHCID 971Oxalic AcidHCID 14798Sodium HydroxideHCID 66658029HCID 66658029、化合物

生成物 1

HCID 580017855-Chloro-6-(hydroxymethyl)-3-pyridinecarbaldehyde収率 10%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Oxalic acid (415 mg, 3.29 mmol) was added to a mixture of [3-chloro-5-(1,3-dioxolan-2-yl)-2-pyridinyl]methanol (142 mg, 0.659 mmol), acetone (7.5 ml), and water (7.5 ml) at room temperature and heated under reflux. After 2.5 h, HPLC showed full conversion. Cooled to rt, basified with 1M NaOH, extracted with TBME, dried (MgSO4), filtered and concentrated to give 139 mg of crude material. Purification by flash chromatography using Flashmaster II, a 5 g silica gel cartridge, and mixtures of DCM and MeOH as eluent afforded impure product. Repurification by manual flash chromatography using a 1 g silica gel cartridge, and mixtures of hexane and EtOAc as eluent afforded 5-chloro-6-(hydroxymethyl)-3-pyridinecarbaldehyde (11.3 mg, 10%) as a white solid.

後処理

  1. temperatureheated
  2. temperatureunder reflux
  3. extractionextracted with TBME
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give 139 mg of crude material
  8. customPurification by flash chromatography
  9. customa 5 g silica gel cartridge, and mixtures of DCM and MeOH as eluent afforded impure product
  10. customRepurification by manual flash chromatography

出典と根拠

ORDレコード
ord-1aa3307aa8d3482fb0ce7a6283c7b964
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08097628B2

反応ノート

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