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Ethanol → Ethyl 5-(hydroxymethyl)picolinate

HRID 501818
ノート
印刷プレビュー

反応式

HRID 501818 の反応式
[BH4-].[Na+].[Cl-].[Ca+2].[Cl-].C(O[C:9]([C:11]1[CH:12]=[CH:13][C:14]([C:17]([OH:19])=[O:18])=[N:15][CH:16]=1)=[O:10])C.S(=O)(=O)(O)O.[CH2:25](O)[CH3:26]>>[OH:10][CH2:9][C:11]1[CH:12]=[CH:13][C:14]([C:17]([O:19][CH2:25][CH3:26])=[O:18])=[N:15][CH:16]=1
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 5

HCID 702Ethanol2 回HCID 1118Sulfuric AcidHCID 5920875-(Ethoxycarbonyl)pyridine-2-carboxylic acidHCID 4311764Sodium borohydrideHCID 5284359Calcium Chloride

生成物 1

HCID 13518564Ethyl 5-(hydroxymethyl)picolinate

実験手順

0.636 g of sodium borohydride was added to 22 mL of ice-cooled ethanol, to which a solution of 1.09 g of calcium chloride in 14 mL of ethanol was added dropwise, followed by addition of 1.20 g of 5-(ethoxycarbonyl)-2-pyridinecarboxylic acid ½ calcium salt, and this mixture was stirred for one hour at room temperature. The reaction mixture, to which 2.8 mL of concentrated sulfuric acid was added, was stirred for 6 hours while heating it under reflux. The reaction mixture was cooled to room temperature and concentrated under reduced pressure followed by successive addition of a saturated aqueous solution of sodium hydrogen carbonate and chloroform, and then the organic phase was separated therefrom. The resultant organic phase was washed with a saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure to yield 0.34 g of ethyl 5-(hydroxymethyl)-2-pyridinecarboxylate as light yellow solid.

後処理

  1. stirringwas stirred for 6 hours
  2. temperaturewhile heating it
  3. temperatureunder reflux
  4. temperatureThe reaction mixture was cooled to room temperature
  5. concentrationconcentrated under reduced pressure
  6. additionfollowed by successive addition of a saturated aqueous solution of sodium hydrogen carbonate and chloroform
  7. customthe organic phase was separated
  8. washThe resultant organic phase was washed with a saturated sodium chloride solution
  9. dry with materialdried over anhydrous magnesium sulfate
  10. distillationthe solvent was distilled out under reduced pressure

出典と根拠

ORDレコード
ord-8aea6389fda448f4b9bb5069139d32a6
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07772285B2

反応ノート

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