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2,4,5-Trichloropyrimidine → 2,5-Dichloro-4-methoxypyrimidine

HRID 410637
Notes
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Reaction equation

HRID 410637 reaction equation
[CH3:1][O-:2].[Na+].[Cl:4][C:5]1[N:10]=[C:9](Cl)[C:8]([Cl:12])=[CH:7][N:6]=1>CO>[Cl:4][C:5]1[N:10]=[C:9]([O:2][CH3:1])[C:8]([Cl:12])=[CH:7][N:6]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 2372592,4,5-TrichloropyrimidineHCID 10942334Sodium Methoxide

Product 1

HCID 497617462,5-Dichloro-4-methoxypyrimidineYield 57.1%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Sodium methoxide (295 mg, 5.45 mmol) was taken up in methanol (13.6 mL) and 2,4,5-trichloropyrimidine (500 mg, 2.73 mmol) was added. The mixture was stirred at room temperature overnight. The resulting mixture was concentrated under reduced pressure. The resulting residue was diluted with diethyl ether, washed with 1:1 water:saturated aqueous ammonium chloride. The organic layer was dried over magnesium sulfate, filtered, and concentrated under reduced pressure. Purification by Chromatography on silica gel (0-10% diethyl ether/hexanes) afforded 2,5-dichloro-4-methoxypyrimidine (280 mg, 1.56 mmol, 57%) as a white solid.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. concentrationThe resulting mixture was concentrated under reduced pressure
  2. additionThe resulting residue was diluted with diethyl ether
  3. washwashed with 1:1 water
  4. dry with materialThe organic layer was dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customPurification by Chromatography on silica gel (0-10% diethyl ether/hexanes)

Sources & evidence

ORD record
ord-506c0e0267bb46e38895ffb9ee233eb4
Source dataset
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08759366B2

Reaction notes

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