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ethyl (2S*,3R*)-2-amino-3-hydroxy-4,4-dimethyl-pentanoate → (2S,3R)-2-Amino-3-Hydroxy-4,4-Dimethylpentanoic Acid

HRID 530576
ノート
印刷プレビュー

反応式

HRID 530576 の反応式
[NH2:1][C@@H:2]([C@H:8]([OH:13])[C:9]([CH3:12])([CH3:11])[CH3:10])[C:3]([O:5]CC)=[O:4]>Cl>[NH2:1][C@@H:2]([C@H:8]([OH:13])[C:9]([CH3:11])([CH3:10])[CH3:12])[C:3]([OH:5])=[O:4]
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

3

反応物 1

HCID 86700026ethyl (2S*,3R*)-2-amino-3-hydroxy-4,4-dimethyl-pentanoate

生成物 1

HCID 2725116(2S,3R)-2-Amino-3-Hydroxy-4,4-Dimethylpentanoic Acid

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

反応条件

温度
130 °C

実験手順

In a round-bottomed flask, ethyl (2S*,3R*)-2-amino-3-hydroxy-4,4-dimethyl-pentanoate (0.596 g, 3.7 mmol) was dissolved in a 6.0 M HCl solution (70 mL). The resulting solution was divided into two equal aliquots and stirred at 130° C. for 1 h. All portions were joined and the reaction mixture extracted with Et2O (3×50 ml). The aqueous phase was concentrated under reduced pressure and the resulting yellowish solid crude product (0.675 g, 93%) was used without further purification in the following reaction. MS (ESI) m/z: 162 [M−H]+; (ESI) m/z: 160 [M−H]−. 1H NMR (DMSO-d6) δ 0.91 (s, 9H), 3.66 (d, J=3.24 Hz, 1H), 3.89 (s, 1H), 5.95 (d, J=6.39 Hz, 1H), 7.92 (s, 3H), 13.88 (s, 1H).

後処理

  1. extractionthe reaction mixture extracted with Et2O (3×50 ml)
  2. concentrationThe aqueous phase was concentrated under reduced pressure
  3. customthe resulting yellowish solid crude product (0.675 g, 93%) was used without further purification in the following reaction

出典と根拠

ORDレコード
ord-5ae4f79ecacb4042bb4aa6c1a0a1e6bb
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09353075B2

反応ノート

読み込み中…

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