Dimethylformamide → 4-(4-Bromo-3-(1,3-dioxolan-2-yl)phenoxy)-3-chlorobenzonitrile

HRID 1664307Notes

Reaction equation

HRID 1664307 reaction equation
[Cl:1][C:2]1[CH:9]=[C:8](F)[CH:7]=[CH:6][C:3]=1C#N.[Br:11][C:12]1[CH:17]=[CH:16][C:15]([OH:18])=[CH:14][C:13]=1[CH:19]1[O:23][CH2:22][CH2:21][O:20]1.C(=O)([O-])[O-].[K+].[K+].C(OCC)(=O)C.O.C[N:38]([CH3:41])C=O>>[Br:11][C:12]1[CH:17]=[CH:16][C:15]([O:18][C:3]2[CH:6]=[CH:7][C:8]([C:41]#[N:38])=[CH:9][C:2]=2[Cl:1])=[CH:14][C:13]=1[CH:19]1[O:20][CH2:21][CH2:22][O:23]1

Participants

6

Reactant 5

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 1090002-Chloro-4-fluorobenzonitrileHCID 22728543Water ethylacetateHCID 579687074-Bromo-3-(1,3-dioxolan-2-yl)phenol

Product 1

HCID 674417784-(4-Bromo-3-(1,3-dioxolan-2-yl)phenoxy)-3-chlorobenzonitrile

Conditions

Temperature
100 °C

Procedure

A mixture of 2-chloro-4-fluorobenzonitrile (4.43 g, 28.4 mmol), 4-bromo-3-(1,3-dioxolan-2-yl)phenol (6.96 g, 28.4 mmol), and potassium carbonate (4.70 g, 34.1 mmol) in N,N-dimethylformamide (60 mL) was stirred at 100° C. under nitrogen atmosphere overnight. The mixture was poured into ethyl acetate/water. The organic layer was washed with brine and dried on anhydrous sodium sulfate. The solvent was removed under reduced pressure to give crude 4-(4-bromo-3-(1,3-dioxolan-2-yl)phenoxy)-3-chlorobenzonitrile (10.8 g), which was used for the next step without purification.

Workup

  1. washThe organic layer was washed with brine
  2. dry with materialdried on anhydrous sodium sulfate
  3. customThe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-e726bd119b8d4485b84377120f96fb5c
Source dataset
uspto-grants-2011_10
Patent number
US08039450B2

Reaction notes

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