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Diisobutylaluminumhydride → 4,5-Dibromofuran-2-carbaldehyde

HRID 271513
ノート
印刷プレビュー

反応式

HRID 271513 の反応式
[H-].C([Al+]CC(C)C)C(C)C.CON(C)[C:14]([C:16]1[O:17][C:18]([Br:22])=[C:19]([Br:21])[CH:20]=1)=[O:15]>O1CCCC1>[Br:21][C:19]1[CH:20]=[C:16]([CH:14]=[O:15])[O:17][C:18]=1[Br: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 21225700DiisobutylaluminumhydrideHCID 446297544,5-Dibromo-N-methoxy-N-methylfuran-2-carboxamide

生成物 1

HCID 10852284,5-Dibromofuran-2-carbaldehyde収率 81%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

Diisobutylaluminum hydride (80 ml, 1M solution in toluene) was added to a solution of the product from Step 2 (20 g, 63.4 mmol) in tetrahydrofuran (160 ml) at −78° C. The mixture was stirred at −78° C. for 1.5 hours and was then quenched with a saturated aqueous solution of ammonium chloride (40 ml). The reaction was allowed to warm to room temperature, diluted with ethyl acetate and 5M hydrochloric acid (20 ml) and stirred for 30 minutes. The organic layer was separated, washed twice with water and then brine, dried and concentrated in vacuo to yield the title compound (12.9 g, 81%); 1H NMR (CDCl3) 9.52 (1H, s), 7.21 (1H, s).

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. customwas then quenched with a saturated aqueous solution of ammonium chloride (40 ml)
  2. temperatureto warm to room temperature
  3. additiondiluted with ethyl acetate and 5M hydrochloric acid (20 ml)
  4. stirringstirred for 30 minutes
  5. customThe organic layer was separated
  6. washwashed twice with water
  7. dry with materialbrine, dried
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-db7036dbb1054244abd4b549c6e7eaf8
出典データセット
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07452906B2

反応ノート

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