Ethane → 1-(4-Bromophenyl)Cyclopropanecarbonitrile

HRID 504351Notes

Reaction equation

HRID 504351 reaction equation
[OH-].[Na+].[Br:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]#[N:12])=[CH:6][CH:5]=1.[CH3:13][CH3:14]>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1>[Br:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2([C:11]#[N:12])[CH2:14][CH2:13]2)=[CH:6][CH:5]=1

Participants

5

Reactant 3

HCID 6324EthaneHCID 14798Sodium HydroxideHCID 27914Benzeneacetonitrile, 4-bromo-

Product 1

HCID 27952731-(4-Bromophenyl)Cyclopropanecarbonitrile

Reagents, catalysts & solvents 1

HCID 66133Benzyl triethylammonium chlorideCatalyst

Procedure

Sodium hydroxide (50% aqueous solution, 29.3 g, 0.505 mol) was added to a mixture of 4-bromo-benzeneacetonitrile (9.80 g, 0.0500 mol), benzyltriethylammonium chloride (0.90 g, 0.0040 mol), ethane, and 1-bromo-2-chloro-(14.5 g, 0.101 mol) at 50° C. overnight. The mixture was poured into ice-water (80 mL) and was extracted with ethyl ether (4×50 mL). The combined organic phase was washed with HCl aqueous solution (1N, 20 mL) and brine (2×30 mL) successively, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was the desired product, which was directly used in the next step without further purification.

Workup

  1. extractionwas extracted with ethyl ether (4×50 mL)
  2. washThe combined organic phase was washed with HCl aqueous solution (1N, 20 mL) and brine (2×30 mL) successively
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customwas directly used in the next step without further purification

Sources & evidence

ORD record
ord-60946d5b91594f25bfc750fe1dd0a0ec
Source dataset
uspto-grants-2010_08
Patent number
US07776874B2

Reaction notes

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