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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
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Acetic Anhydride → (2S)-2-acetamido-3,3-dimethylbutanoic acid

HRID 1260130
ノート
印刷プレビュー

反応式

HRID 1260130 の反応式
[NH2:1][C@H:2]([C:7]([OH:9])=[O:8])[C:3]([CH3:6])([CH3:5])[CH3:4].[C:10](OC(=O)C)(=[O:12])[CH3:11]>C(O)(=O)C>[C:10]([NH:1][C@H:2]([C:7]([OH:9])=[O:8])[C:3]([CH3:6])([CH3:5])[CH3:4])(=[O:12])[CH3:11]
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 7918Acetic AnhydrideHCID 164608L-tert-Leucine

生成物 1

HCID 11469346(2S)-2-acetamido-3,3-dimethylbutanoic acid

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

L-tert-Leucine (manufactured by Tokyo Kasei Kogyo) (4.7 g) was suspended in glacial acetic acid (manufactured by Nakarai Tesk, 40 mL) and heated at 40 to 50° C. together with addition of thrice molar acetic acid anhydride (manufactured by Nakarai Tesk) thereto whereupon the reaction was conducted. After glacial acetic acid was removed in vacuo, the crude crystals were obtained. After that, the crude crystals were recrystallized from 20% isopropyl alcohol. The precipitate was ground in a mortar and dried to give powder of N-acetyl-L-tert-leucine. Details thereof are mentioned in J. P. Greenstein, Chemistry of Amino Acids, 1961, 3.

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

後処理

  1. customAfter glacial acetic acid was removed in vacuo
  2. customthe crude crystals were obtained
  3. customAfter that, the crude crystals were recrystallized from 20% isopropyl alcohol
  4. customdried

出典と根拠

ORDレコード
ord-e27cb2b771654a50b7c924b34b8ba222
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08470574B2

反応ノート

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