ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Potassium Hydroxide → (2E,4E,6E)-3,7,11-trimethyl-2,4,6,10-dodecatetraenoic acid

HRID 1611063
ノート
印刷プレビュー

反応式

HRID 1611063 の反応式
[OH-].[K+].[CH3:3]/[C:4](/[CH:11]=[CH:12]/[CH:13]=[C:14](\[CH3:21])/[CH2:15][CH2:16][CH:17]=[C:18]([CH3:20])[CH3:19])=[CH:5]\[C:6]([O:8]CC)=[O:7]>CC(O)C>[CH3:3]/[C:4](/[CH:11]=[CH:12]/[CH:13]=[C:14](\[CH3:21])/[CH2:15][CH2:16][CH:17]=[C:18]([CH3:20])[CH3:19])=[CH:5]\[C:6]([OH:8])=[O:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14797Potassium HydroxideHCID 6370567ethyl(2E,4E,6E)-3,7,11-trimethyl-2,4,6,10-dodecatetraenoate

生成物 1

HCID 12195841(2E,4E,6E)-3,7,11-trimethyl-2,4,6,10-dodecatetraenoic acid収率 18.6%

試薬・触媒・溶媒 1

HCID 3776Isopropanol溶媒2 回

実験手順

Potassium hydroxide (3.0 g) was dissolved in 30 ml of 2-propanol at 100° C. The solution was added with 2-propanol solution (10 ml) of ethyl (2E,4E,6E)-3,7,11-trimethyl-2,4,6,10-dodecatetraenoate obtained in Example 3 (9.1 g, 34.5 mmol), and stirred at the same temperature for 15 minutes. The reaction mixture was added to ice-water and washed with n-hexane. The solution was neutralized with 10% hydrochloric acid and extracted with n-hexane. The resulting organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was recrystallized from methanol twice to obtain 1.5 g of the title compound (yield 18%) as a yellow crystal.

後処理

  1. washwashed with n-hexane
  2. extractionextracted with n-hexane
  3. washThe resulting organic layer was washed with saturated brine
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent was evaporated under reduced pressure
  6. customThe residue was recrystallized from methanol twice

出典と根拠

ORDレコード
ord-90639ba9cd744325b80804610b48a52e
出典データセット
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06984742B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート