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

Acetyl chloride → 4-Carbomethoxy-2-methylbutanoic acid

HRID 614869
ノート
印刷プレビュー

反応式

HRID 614869 の反応式
CC(CCC(O)=O)C(O)=O.C(Cl)(=O)C.C1(NC2CCCCC2)CCCCC1.[CH3:28][O:29][C:30]([CH2:32][CH2:33][CH:34]([CH3:38])[C:35]([OH:37])=[O:36])=[O:31]>C(OCC)(=O)C>[CH3:28][O:29][C:30]([CH2:32][CH2:33][CH:34]([CH3:38])[C:35]([OH:37])=[O:36])=[O:31]
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 6367Acetyl chlorideHCID 120462-Methylglutaric AcidHCID 705834004-Methoxycarbonyl-2-methyl butanoic acid dicyclohexylamine salt

生成物 1

HCID 131928974-Carbomethoxy-2-methylbutanoic acid

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

2-Methylglutaric acid (14.6 g.) and acetyl chloride (26 ml.) are heated in the steam bath for one hour. The mixture is concentrated to dryness in vacuo and the residue is evaporated twice from toluene. The residue is dissolved in methanol (4.7 ml.) and heated on the steam bath for one hour and concentrated to dryness. The residue is dissolved in a mixture of ether (17 ml.), dicyclohexylamine (16.7 ml.) and hexane (83 ml.). The crystalline salt is filtered off and the filtrate is concentrated to one third volume and chilled. The crystals are filtered and dried to yield 11.3 g. of 4-methoxycarbonyl-2-methyl butanoic acid dicyclohexylamine salt, m.p. 97°-99°. The salt is converted to the free acid by distribution between ethyl acetate and aqueous acid.

後処理

  1. concentrationThe mixture is concentrated to dryness in vacuo
  2. customthe residue is evaporated twice from toluene
  3. dissolutionThe residue is dissolved in methanol (4.7 ml.)
  4. temperatureheated on the steam bath for one hour
  5. concentrationconcentrated to dryness
  6. dissolutionThe residue is dissolved in a mixture of ether (17 ml.), dicyclohexylamine (16.7 ml.) and hexane (83 ml.)
  7. filtrationThe crystalline salt is filtered off
  8. concentrationthe filtrate is concentrated to one third volume
  9. temperaturechilled
  10. filtrationThe crystals are filtered
  11. customdried
  12. customto yield 11.3 g

出典と根拠

ORDレコード
ord-ab940557bcf1458186603e60133c664c
出典データセット
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04146639

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