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Ammonium Chloride → 6-Ethoxy-6-methylheptan-2-OL

HRID 1414828
ノート
印刷プレビュー

反応式

HRID 1414828 の反応式
[CH2:1]([O:3][C:4]([CH3:12])([CH3:11])[CH2:5][CH2:6][CH2:7][C:8](=[O:10])[CH3:9])[CH3:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[NH4+]>C(OCC)C>[CH2:1]([O:3][C:4]([CH3:12])([CH3:11])[CH2:5][CH2:6][CH2:7][CH:8]([OH:10])[CH3:9])[CH3:2]
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

5

反応物 3

HCID 25517Ammonium ChlorideHCID 21226445Aluminium lithium hydrideHCID 214852226-Ethoxy-6-methylheptan-2-one

生成物 1

HCID 227498296-Ethoxy-6-methylheptan-2-OL

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

反応条件

温度
5 °C

実験手順

A solution of 43 g. of 6-ethoxy-6-methyl-2-heptanone in 100 ml. of absolute diethyl ether is slowly added dropwise with ice cooling to a suspension of 4.5 g. of lithium aluminum hydride in 400 ml. of absolute diethyl ether. The mixture is subsequently stirred for a further one hour at ca. 5° C. and then hydrolyzed by the cautious addition of a dilute aqueous ammonium chloride solution. The mixture is filtered through diatomaceous earth and the organic phase washed with saturated sodium chloride solution, dried over sodium sulfate and evaporated under reduced pressure. By distillation there is obtained pure 6-ethoxy-6-methyl-2-heptanol of boiling point 100° C./10 mmHg; nD20 = 1.4372.

後処理

  1. filtrationThe mixture is filtered through diatomaceous earth
  2. washthe organic phase washed with saturated sodium chloride solution
  3. dry with materialdried over sodium sulfate
  4. customevaporated under reduced pressure
  5. distillationBy distillation there

出典と根拠

ORDレコード
ord-316c6cd9a3354cd5b81671d15fed8046
出典データセット
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04002647

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート