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Potassium Hydroxide → (2S)-2-amino-4-fluoro-4-methylpentan-1-ol

HRID 1009265
ノート
印刷プレビュー

反応式

HRID 1009265 の反応式
[F:1][C:2]([CH3:11])([CH3:10])[CH2:3][C@H:4]1[CH2:8][O:7]C(=O)[NH:5]1.[OH-].[K+]>C(O)C>[NH2:5][C@@H:4]([CH2:3][C:2]([F:1])([CH3:11])[CH3:10])[CH2:8][OH:7]
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 14797Potassium HydroxideHCID 11194496(4S)-4-(2-Fluoro-2-methylpropyl)-2-oxazolidinone

生成物 1

HCID 12167160(2S)-2-amino-4-fluoro-4-methylpentan-1-ol

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of the fluoro derivative (21.0 g) from Step 4 in 90% aqueous ethyl alcohol (216 μL) was added potassium hydroxide (21.9 g). The mixture was heated at reflux for 4 hours and cooled to room temperature. The mixture was then concentrated and co-evaporated with toluene (3×300 mL). The residue was dissolved in dichloromethane (500 mL) and stirred for 0.5 hour. The suspension was filtered through celite and the celite was washed with dichloromethane (3×100 mL). The filtrate was concentrated to dryness to yield (2S)-2-amino-4-fluoro-4-methylpentan-1-ol.

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 4 hours
  3. concentrationThe mixture was then concentrated
  4. dissolutionThe residue was dissolved in dichloromethane (500 mL)
  5. filtrationThe suspension was filtered through celite
  6. washthe celite was washed with dichloromethane (3×100 mL)
  7. concentrationThe filtrate was concentrated to dryness

出典と根拠

ORDレコード
ord-89830b8ffcb54425a68b9f11a8b635bd
出典データセット
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07973037B2

反応ノート

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