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Aluminium lithium hydride → N-pentylthiophen-3-amine

HRID 1715219
ノート
印刷プレビュー

反応式

HRID 1715219 の反応式
[S:1]1[CH:5]=[CH:4][C:3]([NH:6][C:7](=O)[CH2:8][CH2:9][CH2:10][CH3:11])=[CH:2]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH2:7]([NH:6][C:3]1[CH:4]=[CH:5][S:1][CH:2]=1)[CH2:8][CH2:9][CH2:10][CH3:11]
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 66725662N-3-thienylpentanamide

生成物 1

HCID 65438924N-pentylthiophen-3-amine収率 79%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
60 °C

実験手順

To a solution of N-3-thienylpentanamide (13.4 g, 73.0 mmol) in THF (200 mL) was added LiAlH4 (3.50 g, 100 mmol) at ambient temperature. The resulting mixture was stirred at ambient temperature for 16 h and at 60° C. for 1 h. After cooling down to ambient temperature, the reaction was quenched by the addition of saturated sodium sulfate dropwise until the color change from green to white and diluted with THF (200 mL). The reaction mixture was filtered through celite and the filtrate was concentrated in vacuo to dryness. The residue was subjected to column chromatography to yield the title compound (9.70 g, 79%): MS (ES+) m/z 170.3 (M+1).

後処理

  1. temperatureAfter cooling down to ambient temperature
  2. customthe reaction was quenched by the addition of saturated sodium sulfate dropwise until the color change from green to white and
  3. additiondiluted with THF (200 mL)
  4. filtrationThe reaction mixture was filtered through celite
  5. concentrationthe filtrate was concentrated in vacuo to dryness

出典と根拠

ORDレコード
ord-0ad2dc16b35a40c5ae8d34ebb73b7adf
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07799798B2

反応ノート

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