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

Sodium Hydroxide → (R)-3-Methylheptanoic acid

HRID 493464
ノート
印刷プレビュー

反応式

HRID 493464 の反応式
[CH3:1][C@@H:2]([CH:7](C(O)=O)[C:8]([OH:10])=[O:9])[CH2:3][CH2:4][CH2:5][CH3:6].[OH-].[Na+]>C1(C)C(C)=CC=CC=1>[CH3:1][C@H:2]([CH2:3][CH2:4][CH2:5][CH3:6])[CH2:7][C:8]([OH:10])=[O:9]
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 2

HCID 14798Sodium HydroxideHCID 11984309HCID 11984309、化合物

生成物 1

HCID 5324547(R)-3-Methylheptanoic acid

試薬・触媒・溶媒 1

HCID 7237O-Xylene溶媒

反応条件

温度
125 °C

実験手順

At room temperature, 60 g of [(R)-1-methylpentyl]-malonic acid (0.318 mol) were dissolved in 120 ml of xylene in a three-neck flask with internal thermometer, condenser and stirrer. The mixture was heated to 125° C. for 5 h. After cooling to 25° C., the mixture was admixed with 200 ml of 2N sodium hydroxide solution. After phase separation, the aqueous phase was admixed with 200 ml of ether and, with cooling, with 180 ml of 15% by weight hydrochloric acid. After phase separation, the aqueous phase was extracted twice with 100 ml of ether. The combined organic phases were washed with 50 ml of water and then dried over sodium sulfate. After solvent had been distilled off, (R)-3-methylheptanoic acid was distilled and obtained in a yield of 35.5 g (77% of theory) with >99% ee and >99% chemical purity (b.p.: 67-68° C. at 0.45 mbar).

後処理

  1. temperatureAfter cooling to 25° C.
  2. customAfter phase separation
  3. temperaturewith cooling, with 180 ml of 15% by weight hydrochloric acid
  4. customAfter phase separation
  5. extractionthe aqueous phase was extracted twice with 100 ml of ether
  6. washThe combined organic phases were washed with 50 ml of water
  7. dry with materialdried over sodium sulfate
  8. distillationAfter solvent had been distilled off
  9. distillation(R)-3-methylheptanoic acid was distilled
  10. customobtained in a yield of 35.5 g (77% of theory) with >99% ee and >99% chemical purity (b.p.: 67-68° C. at 0.45 mbar)

出典と根拠

ORDレコード
ord-ee3a769c614d4b6d876bb3dfdcbc7f59
出典データセット
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07534908B2

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