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

HCID 54518938、化合物 → Ethyl (2R)-2,3-dihydroxy-2-methylpropanoate

HRID 262053
ノート
印刷プレビュー

反応式

HRID 262053 の反応式
C([O:8][C@:9]([CH3:17])([CH2:15][OH:16])[C:10]([O:12][CH2:13][CH3:14])=[O:11])C1C=CC=CC=1.[H][H]>C(OCC)(=O)C.[Pd]>[OH:8][C@:9]([CH3:17])([CH2:15][OH:16])[C:10]([O:12][CH2:13][CH3:14])=[O:11]
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 2

HCID 54518938HCID 54518938、化合物HCID 178418361HCID 178418361、化合物2 回

生成物 1

HCID 53737198Ethyl (2R)-2,3-dihydroxy-2-methylpropanoate収率 92.8%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 8857Ethyl Acetate溶媒

実験手順

22 g of ethyl (R)-2-benzyloxy-3-hydroxy-2-methyl-propionate (manufactured in accordance with Example 1) in 150 ml of ethyl acetate were hydrogenated with hydrogen gas in the presence of 11 g of 5% by weight palladium/carbon catalyst up to the cessation of the hydrogen uptake. The catalyst was filtered off, washed with ethyl acetate (2×50 ml), the filtrate was concentrated in the vacuum and the residual oil was distilled at 56-57°/0.1 mmHg. There were obtained 12.7 g of ethyl (R)-2,3-dihydroxy-2-methyl-propionate in the form of a colorless viscous liquid. [α]D =+0.339° (undiluted);=+11.6° (c=2.12 in chloroform).

後処理

  1. filtrationThe catalyst was filtered off
  2. washwashed with ethyl acetate (2×50 ml)
  3. concentrationthe filtrate was concentrated in the vacuum
  4. distillationthe residual oil was distilled at 56-57°/0.1 mmHg

出典と根拠

ORDレコード
ord-c582f80c0d44427d912b3871bdd53dc5
出典データセット
uspto-grants-1979_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04153614

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