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

HRID 1260130
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HRID 1260130 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 164608L-tert-Leucine

생성물 1

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

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-e27cb2b771654a50b7c924b34b8ba222
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08470574B2

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