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Water → 4-Amino-3-bromo-2,5-difluorobenzonitrile

HRID 389519
ノート
印刷プレビュー

反応式

HRID 389519 の反応式
[Br:1]Br.O.[NH2:4][C:5]1[C:12]([F:13])=[CH:11][C:8]([C:9]#[N:10])=[C:7]([F:14])[CH:6]=1>C(O)(=O)C>[NH2:4][C:5]1[C:12]([F:13])=[CH:11][C:8]([C:9]#[N:10])=[C:7]([F:14])[C:6]=1[Br:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 24408BromineHCID 27359004-Amino-2,5-difluorobenzonitrile

生成物 1

HCID 146210194-Amino-3-bromo-2,5-difluorobenzonitrile収率 93.9%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A mixture of bromine (1.65 mL, 32 mmol), water (2 mL), and 4-amino-2,5-difluorobenzonitrile (5 g, 32 mmol) in acetic acid (50 mL) was stirred at RT for 16 h. The mixture was poured into ice cooled saturated sodium bicarbonate solution, causing a solid to separate out. The solid was filtered and washed with water. The solid was then dissolved in DCM, washed with water, dried over sodium sulfate, filtered, and concentrated to afford 7 g (92%) of the title compound. 1H NMR (300 MHz, CDCl3): δ 7.18-7.21 (m, 1H), 4.80 (br. s, 2H).

後処理

  1. additionThe mixture was poured into ice cooled saturated sodium bicarbonate solution
  2. customto separate out
  3. filtrationThe solid was filtered
  4. washwashed with water
  5. dissolutionThe solid was then dissolved in DCM
  6. washwashed with water
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-462d0895a7ef4bb5b090541c1dc150e0
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08378104B2

反応ノート

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