Pyridine → 2-Bromoethyl 4-nitrobenzoate

HRID 1250339Notes

Reaction equation

HRID 1250339 reaction equation
[Br:1][CH:2](O)[CH3:3].N1C=CC=CC=1.[N+:11]([C:14]1[CH:22]=[CH:21][C:17]([C:18](Cl)=[O:19])=[CH:16][CH:15]=1)([O-:13])=[O:12].CC[O:25]CC>>[Br:1][CH2:2][CH2:3][O:19][C:18](=[O:25])[C:17]1[CH:21]=[CH:22][C:14]([N+:11]([O-:13])=[O:12])=[CH:15][CH:16]=1

Participants

5

Reactant 4

HCID 1049PyridineHCID 3283Diethyl Ether3×HCID 85024-Nitrobenzoyl chlorideHCID 14202443Ethanol, 1-bromo-

Product 1

HCID 2803962-Bromoethyl 4-nitrobenzoate

Procedure

Under a nitrogen atmosphere, bromoethanol (29 mmols) was dissolved in 25 mL ether. Pyridine (34 mmols) was added to the solution, followed by a solution of 4-nitrobenzoyl chloride (27 mmols) in 35 mL ether. The reaction was stirred overnight, and a white precipitate was formed. Ether (50 mL) was added, and the reaction mixture was then washed with aqueous KHSO4, aqueous NaHCO3, and water. The ether layer was then dried over Na2SO4, filtered, and concentrated to give 6.3 g of 4-nitrobenzoic acid 2-bromo-ethyl ester. Material was used in coupling reactions without further purification.

Workup

  1. customa white precipitate was formed
  2. washthe reaction mixture was then washed with aqueous KHSO4, aqueous NaHCO3, and water
  3. dry with materialThe ether layer was then dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-6ab78bdfa16b49f1b0686d674ff20e5f
Source dataset
uspto-grants-2002_01
Patent number
US06337423B1

Reaction notes

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