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dimethyl 3-methyl-L-aspartate → (2S)-2-amino-4-methoxy-3-methyl-4-oxobutanoic acid

HRID 1424213
ノート
印刷プレビュー

反応式

HRID 1424213 の反応式
[CH3:1][CH:2]([C:9]([O:11][CH3:12])=[O:10])[C@@H:3]([C:5]([O:7]C)=[O:6])[NH2:4].[NH4+]=S>O.C([O-])([O-])=O.O.O.[Cu].[Cu+2]>[NH2:4][C@@H:3]([CH:2]([CH3:1])[C:9]([O:11][CH3:12])=[O:10])[C:5]([OH:7])=[O:6]
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 1

HCID 86699126dimethyl 3-methyl-L-aspartate

生成物 1

HCID 86699124(2S)-2-amino-4-methoxy-3-methyl-4-oxobutanoic acid

試薬・触媒・溶媒 2

HCID 10922056HCID 10922056、化合物触媒HCID 962Water溶媒

反応条件

温度
70 °C

実験手順

A mixture of dimethyl 3-methyl-L-aspartate (Preparation 64, 23 g, 82.55 mmol), CuCO3.Cu(OH)2 (21.9 g, 99.05 mmol) in water (250 mL) was heated to 70° C. for 4 hours. The resulting precipitate was filtered and the filtrate cooled to 0° C. Ammonium sulfide (20% in water, 67.5 mL, 198 mmol) was added slowly ensuring the temperature did not rise above 5° C. The reaction was filtered through arbocel to remove the copper residues and the filtrate concentrated in vacuo. The residue was redissolved in MeOH and filtered through arbocel, with concentration of the filtrate to dryness to afford the title compound as an oil that was used directly in the next step.

後処理

  1. filtrationThe resulting precipitate was filtered
  2. temperaturethe filtrate cooled to 0° C
  3. customdid not rise above 5° C
  4. filtrationThe reaction was filtered through arbocel
  5. customto remove the copper residues
  6. concentrationthe filtrate concentrated in vacuo
  7. dissolutionThe residue was redissolved in MeOH
  8. filtrationfiltered through arbocel, with concentration of the filtrate to dryness

出典と根拠

ORDレコード
ord-aa131b17a9a447f68494f857fa7965ea
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08927587B2

反応ノート

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