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Diisobutylaluminum hydride → HCID 39232332、化合物

HRID 1889714
ノート
印刷プレビュー

反応式

HRID 1889714 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:13]([Cl:14])=[CH:12][CH:11]=[C:10]([C:15](N(OC)C)=[O:16])[CH:9]=2)=[CH:4][CH:3]=1.CC(C[AlH]CC(C)C)C>C1COCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:13]([Cl:14])=[CH:12][CH:11]=[C:10]([CH:15]=[O:16])[CH:9]=2)=[CH:4][CH:3]=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 58531623HCID 58531623、化合物

生成物 1

HCID 39232332HCID 39232332、化合物収率 87.1%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

4′,6-Dichloro-N-methoxy-N-methylbiphenyl-3-carboxamide (1.0 g, 3.2 mmol, 1.0 eq) was dissolved in dry THF and stirred for 10 minutes. The solution was cooled to −78° C. and DIBAL-H (1 M solution, 1.83 g, 12.9 mmol, 4 eq, 13 mL) was slowly added over 15-30 minutes. The reaction mixture was stirred for 1 h at −78° C., quenched with saturated NH4Cl solution at −78° C. and stirred for 30 minutes at ambient temperature. Water and ethyl acetate were added into the reaction mixture. The aqueous layer was separated and extracted twice with ethyl acetate. The organic layer was dried with anhydrous Na2SO4 and concentrated under vacuum to give the desired product (0.7 g, 87%). 1H NMR (400 MHz, CDCl3) δ 7.06-7.09 (d, 2H), 7.24-7.27 (d, 2H), 7.40 (s, 1H), 7.55-7.58 (d, 1H), 7.90-7.95 (m, 1H).

後処理

  1. stirringThe reaction mixture was stirred for 1 h at −78° C.
  2. customquenched with saturated NH4Cl solution at −78° C.
  3. stirringstirred for 30 minutes at ambient temperature
  4. additionWater and ethyl acetate were added into the reaction mixture
  5. customThe aqueous layer was separated
  6. extractionextracted twice with ethyl acetate
  7. dry with materialThe organic layer was dried with anhydrous Na2SO4
  8. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-2f5ba791826e4ac0b37ff84529f555f9
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08501992B2

反応ノート

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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