Dichloromethane → HCID 21914164, compound

HRID 434156Notes

Reaction equation

HRID 434156 reaction equation
ClCCl.[C:4]([C:6]1[CH:7]=[C:8](B(O)O)[CH:9]=[CH:10][CH:11]=1)#[N:5].Br[C:16]1[CH:21]=[C:20]([N+:22]([O-:24])=[O:23])[CH:19]=[CH:18][C:17]=1[O:25][CH3:26].C(=O)([O-])[O-].[Cs+].[Cs+]>COCCOC.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[C:4]([C:6]1[CH:7]=[C:8]([C:18]2[CH:19]=[C:20]([N+:22]([O-:24])=[O:23])[CH:21]=[CH:16][C:17]=2[O:25][CH3:26])[CH:9]=[CH:10][CH:11]=1)#[N:5]

Participants

7

Conditions

Temperature
90 °C

Procedure

[1,1′Bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane (1:1) (1.43 g) was added to a stirred mixture of 3-cyanophenylboronic acid (10.0 g, 61.8 mmol) and 2-bromo-4-nitroanisole (14.35 g, 62 mmol) in 2.0N cesium carbonate (92.7 mL, 185.4 mmol) and ethylene glycol dimethylether (200 mL). The flask was purged with nitrogen and heated at 90° C. (oil bath) for 4 hours. The mixture was allowed to cool to room temperature overnight, during which time the product precipitated from solution. The solid was collected on a Buchner funnel, washed with water and dried under reduced pressure to give 2-(3-cyanophenyl)-4-nitroanisole (15.7 g).

Workup

  1. customThe flask was purged with nitrogen
  2. temperatureto cool to room temperature overnight, during which time the product
  3. customprecipitated from solution
  4. customThe solid was collected on a Buchner funnel
  5. washwashed with water
  6. customdried under reduced pressure

Sources & evidence

ORD record
ord-605541a9169948d79ae571fee197a1d3
Source dataset
uspto-grants-2003_12
Patent number
US06670376B1

Reaction notes

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