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Benzene → 3-Bromo-2-chloro-4,5-difluorobenzonitrile

HRID 414381
ノート
印刷プレビュー

反応式

HRID 414381 の反応式
F[B-](F)(F)F.[Br:6][C:7]1[C:8]([Cl:17])=[C:9]([N+]#N)[CH:10]=[C:11]([F:14])[C:12]=1[F:13].[C-:18]#[N:19].[K+].C(=O)([O-])[O-].[Na+].[Na+].C1C=CC=CC=1>O>[Br:6][C:7]1[C:8]([Cl:17])=[C:9]([CH:10]=[C:11]([F:14])[C:12]=1[F:13])[C:18]#[N:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 241BenzeneHCID 9032Potassium CyanideHCID 10340Sodium CarbonateHCID 143652533-Bromo-2-chloro-4,5-difluorobenzenediazonium tetrafluoroborate

生成物 1

HCID 140717963-Bromo-2-chloro-4,5-difluorobenzonitrile収率 41.4%

試薬・触媒・溶媒 1

HCID 962Water
溶媒

実験手順

3-Bromo-2-chloro-4,5-difluorobenzenediazonium tetrafluoroborate (35.6 g) was added portionwise during 40 minutes to a solution of cuprous cyanide (18.67 g), potassium cyanide (27.14 g) and sodium carbonate (5.52 g) in water (200 ml) with stirring vigorously at room temperature. After the mixture was stirred for 4.5 hours, benzene (250 ml) was added to the suspension and then the mixture was stirred for 25 minutes. The insoluble materials were collected by filtration, and washed with benzene. The filtrate and washings were combined and washed with water, dried over ahhydrous sodium sulfate and then concentrated. The resulting residue was purified by silica gel chromatography eluting with dichloromethane-n-hexane (1:3) and further recrystallized from n-hexane-dichloromethane to give the title compound (10.9 g) as light yellow needles, mp 71°-72.5° C.

後処理

  1. stirringAfter the mixture was stirred for 4.5 hours
  2. stirringthe mixture was stirred for 25 minutes
  3. filtrationThe insoluble materials were collected by filtration
  4. washwashed with benzene
  5. washwashed with water
  6. dry with materialdried over ahhydrous sodium sulfate
  7. concentrationconcentrated
  8. customThe resulting residue was purified by silica gel chromatography
  9. washeluting with dichloromethane-n-hexane (1:3)
  10. customfurther recrystallized from n-hexane-dichloromethane

出典と根拠

ORDレコード
ord-6cbf514b19e341c28406dc1df601f55f
出典データセット
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04791225

反応ノート

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