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Hydrochloric Acid → 1-Propanol, 2-(octyloxy)-

HRID 1885108
ノート
印刷プレビュー

反応式

HRID 1885108 の反応式
[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH2:7]([O:15][CH:16]([CH3:22])[C:17](OCC)=[O:18])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].Cl>C(OCC)C>[CH2:7]([O:15][CH:16]([CH3:22])[CH2:17][OH:18])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]
参加物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 313Hydrochloric Acid2 回HCID 14692867HCID 14692867、化合物HCID 21226445Aluminium lithium hydride

生成物 1

HCID 100582981-Propanol, 2-(octyloxy)-収率 86.3%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

Then, 7.5 g of LiAlH4 was added to 250 ml of diethyl ether, followed by stirring for a little while. Then, a solution of 56 g of the above ester in 50 ml of diethyl ether was added dropwise in 2 hours at below 5° C. After the addition, the mixture was stirred at room temperature for 2 hours and allowed to stand for 15 hours. After the reaction, 30 ml of 5% hydrochloric acid was added, and 6N-hydrochloric acid was added to provide a pH of about 1, followed by extraction with ether. The product was washed with water, dried and subjected to removal of the solvent by distillation, followed by vacuum distillation to obtain 39.5 g of 2-octyloxypropanol as a fraction of 107° C./3 mmHg.

後処理

  1. additionAfter the addition
  2. stirringthe mixture was stirred at room temperature for 2 hours
  3. additionwas added
  4. customto provide a pH of about 1
  5. extractionfollowed by extraction with ether
  6. washThe product was washed with water
  7. customdried
  8. customsubjected to removal of the solvent by distillation
  9. distillationfollowed by vacuum distillation

出典と根拠

ORDレコード
ord-25c19f88f67b4793b62715c58c1810b4
出典データセット
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05143643

反応ノート

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