Dichloromethane → HCID 21914164, compound

HRID 1988306Notes

Reaction equation

HRID 1988306 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.Cl[Pd]Cl.C1(P(C2C=CC=CC=2)[C-]2C=CC=C2)C=CC=CC=1.[C-]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=C1.[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-a0061fde0f044923ad3f88ed2613c7eb
Source dataset
uspto-grants-2009_06
Patent number
US07553971B2

Reaction notes

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