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Methyl iodide → (2S,3R)-2-{[(tert-butoxy)carbonyl]amino}-3-methoxybutanoic acid

HRID 427386
ノート
印刷プレビュー

反応式

HRID 427386 の反応式
[NH:1]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[C@H:2]([C:6]([OH:8])=[O:7])[C@@H:3]([CH3:5])[OH:4].[H-].[Na+].[CH3:18]I>C1COCC1>[NH:1]([C:9]([O:11][C:12]([CH3:14])([CH3:13])[CH3:15])=[O:10])[C@H:2]([C:6]([OH:8])=[O:7])[C@@H:3]([CH3:5])[O:4][CH3:18]
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 6328Methyl iodideHCID 24758Sodium hydrideHCID 2724766N-tert-Butoxycarbonyl-L-threonine

生成物 1

HCID 15460346(2S,3R)-2-{[(tert-butoxy)carbonyl]amino}-3-methoxybutanoic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

In a THF solution containing 0.8 g of Boc-Thr-OH, 100 mg of sodium hydride (60% in oil) was added under ice cooling and the resultant mixture was stirred for 30 min at room temperature. Further, 2.8 ml of methyl iodide was added and the obtained reaction mixture was stirred overnight at room temperature. The reaction mixture was evaporated under reduced pressure and the resultant residue was redissolved in ethyl acetate, washed with 5% sodium hydrogensulfite aqueous solution, water and saturated sodium chloride aqueous solution, successively, and dried over anhydrous sodium sulfate. The dried solution was evaporated under reduced pressure, dissolved in methanol, mixed with DCHA and reevaporated. Ether-hexane was added to the residue to give 0.55 g of the title compound as its DCHA salt.

後処理

  1. additionwas added under ice cooling
  2. customthe obtained reaction mixture
  3. customThe reaction mixture was evaporated under reduced pressure
  4. dissolutionthe resultant residue was redissolved in ethyl acetate
  5. washwashed with 5% sodium hydrogensulfite aqueous solution, water and saturated sodium chloride aqueous solution
  6. dry with materialsuccessively, and dried over anhydrous sodium sulfate
  7. customThe dried solution was evaporated under reduced pressure
  8. dissolutiondissolved in methanol
  9. additionmixed with DCHA
  10. customreevaporated
  11. additionEther-hexane was added to the residue

出典と根拠

ORDレコード
ord-993ac4fef23748b9b84fc2b29d088d4b
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06313094B1

反応ノート

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