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HCID 58017434、化合物 → 2-Amino-3-(oxan-3-yl)propan-1-ol

HRID 451854
ノート
印刷プレビュー

反応式

HRID 451854 の反応式
[NH:1]([C@@H:3]([CH2:6][CH:7]1[CH2:12][CH2:11][CH2:10][O:9][CH2:8]1)[CH2:4][OH:5])N>CO.[Ni]>[NH2:1][C@@H:3]([CH2:6][CH:7]1[CH2:12][CH2:11][CH2:10][O:9][CH2:8]1)[CH2:4][OH:5]
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 1

HCID 58017434HCID 58017434、化合物

生成物 1

HCID 509986342-Amino-3-(oxan-3-yl)propan-1-ol収率 102.8%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 887Methanol溶媒

実験手順

To the solution of (2S)-2-hydrazinyl-3-(tetrahydro-2H-pyran-3-yl)propan-1-ol (5.79 g, 0.033 mol) in MeOH (100 mL) was added Raney Ni. The flask was degassed and equipped with a hydrogen inflated balloon. The flask was dipped into an ultrasound bath filled with water and sonicated for 4 hr at rt until the starting material was completely consumed. The mixture was then filtered through celite, and the filter cake was washed with MeOH (2×30 mL). Removal under reduced pressure gave (2S)-2-amino-3-(tetrahydro-2H-pyran-3-yl)propan-1-ol (5.4 g, 90%).

後処理

  1. customThe flask was degassed
  2. customequipped with a hydrogen inflated balloon
  3. customThe flask was dipped into an ultrasound bath
  4. additionfilled with water
  5. customsonicated for 4 hr at rt until the starting material
  6. customwas completely consumed
  7. filtrationThe mixture was then filtered through celite
  8. washthe filter cake was washed with MeOH (2×30 mL)
  9. customRemoval under reduced pressure

出典と根拠

ORDレコード
ord-c4c015bc6501412cb877396c4ede027d
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08487108B2

反応ノート

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