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Ethanol → Ethyl 6-(hydroxymethyl)pyridine-3-carboxylate

HRID 1612035
ノート
印刷プレビュー

反応式

HRID 1612035 の反応式
[N:1]1[CH:6]=[C:5]([C:7]([O-:9])=[O:8])[CH:4]=[CH:3][C:2]=1[C:10]([O:12]CC)=O.[BH4-].[Na+].[Cl-].[Ca+2].[Cl-].O.[CH2:21](O)[CH3:22]>>[OH:12][CH2:10][C:2]1[CH:3]=[CH:4][C:5]([C:7]([O:9][CH2:21][CH3:22])=[O:8])=[CH:6][N:1]=1
参加物反応条件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 702EthanolHCID 962WaterHCID 4311764Sodium borohydrideHCID 5284359Calcium ChlorideHCID 425440302,5-Pyridinedicarboxylic acid, 2-ethyl ester

生成物 1

HCID 15045504Ethyl 6-(hydroxymethyl)pyridine-3-carboxylate収率 84%

反応条件

温度
-5 °C

実験手順

45.77 g (205 mmol) of ethyl 2,5-pyridine-dicarboxylate was dissolved in 410 ml of absolute ethanol in a one-liter round-bottomed flask. The reaction medium was cooled to −5° C. and 5.04 g (133.2 mmol) of sodium borohydride was added, followed by portionwise addition of 14.79 g (133.2 mmol) of calcium chloride, while keeping the temperature below −5° C. The reaction medium was stirred at −5° C. for two hours and poured into water. The product was extracted with ethyl ether and washed with water and the organic phase was then dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a column of silica eluted with ethyl ether, in order to obtain 31.33 g (84%) of a white crystalline solid.

後処理

  1. customthe temperature below −5° C
  2. extractionThe product was extracted with ethyl ether
  3. washwashed with water
  4. dry with materialthe organic phase was then dried over magnesium sulfate
  5. customevaporated
  6. customThe residue obtained
  7. customwas purified by chromatography on a column of silica
  8. washeluted with ethyl ether, in order

出典と根拠

ORDレコード
ord-4db1771cc3784819856695f8385d42d5
出典データセット
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06992095B2

反応ノート

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