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3-Hydroxybutyric Acid → Dodecyl 3-Hydroxybutyrate

HRID 2380182
ノート
印刷プレビュー

反応式

HRID 2380182 の反応式
[OH:1][CH:2]([CH3:7])[CH2:3][C:4]([OH:6])=[O:5].[CH2:8](O)[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19].S(=O)(=O)(O)O>>[OH:1][CH:2]([CH3:7])[CH2:3][C:4]([O:6][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH3:8])=[O:5]
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

4

反応物 3

HCID 4413-Hydroxybutyric AcidHCID 1118Sulfuric AcidHCID 81931-Dodecanol

生成物 1

HCID 18955122Dodecyl 3-Hydroxybutyrate収率 117.65%

反応条件

温度
120 °C

実験手順

A 500 mL one neck round bottom flask equipped with a Dean Stark trap, condenser, and a nitrogen inlet/outlet was charged with 72.0 g (69 mmole) of 3-hydroxybutyric acid, 268.5 g (1.45 mole) of dodecyl alcohol, and 0.36 g of sulfuric acid. The mixture was heated to 120° C. for 48 hours and water was collected as the reaction proceeded. The acid was neutralized by washing three times with 100 mL saturated NaHCO3 solution. The organic layer was collected and dried over MgSO4 and concentrated. Excess dodecanol was removed by high vacuum distillation to yield 117.65% (60% yield) of clear oil (91% pure by GC).

後処理

  1. customwater was collected as the reaction
  2. washby washing three times with 100 mL saturated NaHCO3 solution
  3. customThe organic layer was collected
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. customExcess dodecanol was removed by high vacuum distillation

出典と根拠

ORDレコード
ord-42787cf725b047e0bc59a10aa1987dc9
出典データセット
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05366665

反応ノート

読み込み中…

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