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Formic Acid → 4-Amino-3-bromo-2,5-difluorobenzaldehyde

HRID 577289
ノート
印刷プレビュー

反応式

HRID 577289 の反応式
[NH2:1][C:2]1[C:9]([F:10])=[CH:8][C:5]([C:6]#N)=[C:4]([F:11])[C:3]=1[Br:12].C(O)=[O:14]>[Ni]>[NH2:1][C:2]1[C:9]([F:10])=[CH:8][C:5]([CH:6]=[O:14])=[C:4]([F:11])[C:3]=1[Br:12]
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 284Formic AcidHCID 146210194-Amino-3-bromo-2,5-difluorobenzonitrile

生成物 1

HCID 146210204-Amino-3-bromo-2,5-difluorobenzaldehyde収率 83%

試薬・触媒・溶媒 1

HCID 935Nickel触媒

反応条件

温度
85 °C

実験手順

Raney nickel (5.3 g, 50% slurry in water) was added to a solution of 4-amino-3-bromo-2,5-difluoro-benzonitrile (4.0 g, 17.2 mmol) in formic acid (60 mL). After heating for 1 h at 85° C., the reaction mixture was filtered through Celite, washed with DCM and evaporated to dryness. The residue was suspended in DCM and neutralized carefully with saturated sodium hydrogencarbonate. The aqueous phase was extracted with DCM and the combined organic phases were dried over sodium sulfate and evaporated to yield 4-amino-3-bromo-2,5-difluorobenzaldehyde (3.4 g, 14.3 mmol, 83%). 1H NMR (d6-DMSO) δ 9.91 (d, J=3.0 Hz, 1H), 7.45 (dd, J=11.0, 6.0 Hz, 1H), 6.96 (br s, 2H).

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. filtrationthe reaction mixture was filtered through Celite
  2. washwashed with DCM
  3. customevaporated to dryness
  4. extractionThe aqueous phase was extracted with DCM
  5. dry with materialthe combined organic phases were dried over sodium sulfate
  6. customevaporated

出典と根拠

ORDレコード
ord-dfb3979bdad84820bfc7bb55d0fa723e
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09040545B2

反応ノート

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