Sodium Hydroxide → 3-Bromo-5-(trifluoromethyl)pyridin-2-amine

HRID 2414449Notes

Reaction equation

HRID 2414449 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][N:3]=1.[Br:12]Br.[OH-].[Na+]>C(O)(=O)C.CCOCC>[NH2:1][C:2]1[C:7]([Br:12])=[CH:6][C:5]([C:8]([F:9])([F:11])[F:10])=[CH:4][N:3]=1

Participants

6

Reactant 3

HCID 14798Sodium HydroxideHCID 24408BromineHCID 7358622-Amino-5-(trifluoromethyl)pyridine

Product 1

HCID 130641553-Bromo-5-(trifluoromethyl)pyridin-2-amine

Reagents, catalysts & solvents 2

HCID 176Acetic AcidSolventHCID 3283Diethyl EtherSolvent

Procedure

To a solution of 2-amino-5-trifluoromethylpyridine (9 g) in acetic acid (75 mL) at r.t. was added bromine (5.8 mL) slowly. After 1 h, the acid was neutralized by the careful addition of sodium hydroxide (10 N) at 0° C. The resulting orange precipitate was dissolved in ether and washed successively with saturated potassium carbonate, saturated Na2SO3 and brine, dried and concentrated. The residual solid was stirred vigorously in hexane for 1 h to provide, after filtration, the title compound as a white solid (10.2 g).

Workup

  1. washwashed successively with saturated potassium carbonate, saturated Na2SO3 and brine
  2. customdried
  3. concentrationconcentrated
  4. customto provide
  5. filtrationafter filtration

Sources & evidence

ORD record
ord-56ca0318df4d4afea256494cf66f4ffc
Source dataset
uspto-grants-2004_11
Patent number
US06812346B2

Reaction notes

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