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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Diisobutylaluminum hydride → HCID 14948472、化合物

HRID 570997
ノート
印刷プレビュー

反応式

HRID 570997 の反応式
[CH3:1][N:2]([CH3:10])[C:3](=O)[CH:4]([CH2:7][Br:8])[CH2:5][Br:6].CC(C[AlH]CC(C)C)C>C(Cl)Cl>[Br:6][CH2:5][CH:4]([CH2:7][Br:8])[CH2:3][N:2]([CH3:10])[CH3:1]
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 14487Diisobutylaluminum hydrideHCID 144423013-Bromo-2-(bromomethyl)-N,N-dimethylpropanamide

生成物 1

HCID 14948472HCID 14948472、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
-10 °C

実験手順

To a solution of N,N-dimethyl-3-bromo-2-(bromomethyl) proprionic amide (44 g) in CH2Cl2 (300 mL) was added DIBAL (450 mL, 1.0 M in toluene) at −40° C. over 30 minutes. The mixture was allowed to warm to −10° C. over 3 hours and the diluted with CH2Cl2 (1500 mL). The reaction was quenched with a mixture of water (300 mL) and methanol (100 mL) at −10° C., followed by stirring at a temperature less that 10° C. for 2 hours. The suspension was filtered, dried, and concentrated to ca. 300 mL. The product crystallized upon standing overnight at room temperature. The crystals were separated from the solution and dried (19 g, 66%). MS(M+1): 178.

後処理

  1. customThe reaction was quenched with a mixture of water (300 mL) and methanol (100 mL) at −10° C.
  2. filtrationThe suspension was filtered
  3. customdried
  4. concentrationconcentrated to ca. 300 mL
  5. customThe product crystallized
  6. waitupon standing overnight at room temperature
  7. customThe crystals were separated from the solution
  8. customdried (19 g, 66%)

出典と根拠

ORDレコード
ord-1a61fb269e9f4ee5837988d13d32f1ae
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09024028B2

反応ノート

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