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Aluminium lithium hydride → (S)-(1,4-Dimethylpiperazin-2-YL)methanol

HRID 2262467
ノート
印刷プレビュー

反応式

HRID 2262467 の反応式
C(O[C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14](OC(C)(C)C)=O)[CH2:10][C@H:9]1[CH2:21][OH:22])=O)(C)(C)C.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH3:6][N:8]1[CH2:13][CH2:12][N:11]([CH3:14])[CH2:10][C@H:9]1[CH2:21][OH:22]
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

4

反応物 2

HCID 21226445Aluminium lithium hydrideHCID 66934642(S)-DI-Tert-butyl 2-(hydroxymethyl)piperazine-1,4-dicarboxylate

生成物 1

HCID 7035990(S)-(1,4-Dimethylpiperazin-2-YL)methanol収率 56%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

(S)-2-hydroxymethyl-piperazine-1,4-dicarboxylic acid di-tert-butyl ester (5.66 g, 17.9 mmol) was dissolved in THF (10 mL) and cooled to 0° C. 2M LiAlH4 in THF (28.5 mL, 57.0 mmol) was added. The reaction mixture was stirred at reflux for 4 hours and then cooled to 0° C. and quenched with the drop-wise addition of 1M sodium hydroxide solution (20 mL). The reaction mixture was diluted with THF (50 mL), filtered and the filtrate was concentrated in vacuo to give 1,4-dimethyl-(S)-2-hydroxymethyl piperazine (1.44 g, 56%) as a colourless oil which was used without further purification.

後処理

  1. temperatureat reflux for 4 hours
  2. temperaturecooled to 0° C.
  3. customquenched with the drop-wise addition of 1M sodium hydroxide solution (20 mL)
  4. additionThe reaction mixture was diluted with THF (50 mL)
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-2ecdd282e637496e876d256bafccafac
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07851471B2

反応ノート

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