Sodium Hydroxide → 3-Amino-1-(thiophen-3-yl)propan-1-ol

HRID 1809674ノート

反応式

HRID 1809674 の反応式
[H-].[H-].[H-].[H-].[Li+].[Al+3].[O:7]=[C:8]([C:12]1[CH:16]=[CH:15][S:14][CH:13]=1)[CH2:9][C:10]#[N:11].[OH-].[Na+]>C1COCC1>[NH2:11][CH2:10][CH2:9][CH:8]([C:12]1[CH:16]=[CH:15][S:14][CH:13]=1)[OH:7]

参加物

5

反応物 3

HCID 14798Sodium HydroxideHCID 27400753-Oxo-3-(thiophen-3-yl)propanenitrileHCID 21226445Aluminium lithium hydride

生成物 1

HCID 651850053-Amino-1-(thiophen-3-yl)propan-1-ol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
25 °C

実験手順

To a stirred suspension of LAH (1.45 g, 38.1 mmol) in dry THF (120 mL) was added a solution of 3-oxo-3-(thiophen-3-yl)propanenitrile (4.8 g, 31.8 mmol) in dry THF (40 mL) dropwise at 0° C. under nitrogen atmosphere. The mixture was warmed to 25° C. and then heated at 65° C. for 6 hours. After cooling to 0° C., a saturated solution of sodium hydroxide (2 mL) was added dropwise and the mixture was filtered. The filtrate was concentrated to dryness to give crude 3-amino-1-thiophen-3-yl-propan-1-ol which was used in next step without further purification.

後処理

  1. temperatureheated at 65° C. for 6 hours
  2. temperatureAfter cooling to 0° C.
  3. filtrationthe mixture was filtered
  4. concentrationThe filtrate was concentrated to dryness

出典と根拠

ORDレコード
ord-349e82b266b44e12810cfc41df88d149
出典データセット
uspto-grants-2013_01
特許番号
US08362023B2

反応ノート

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