Sodium hydride → 4-Chloro-6-(1-methyl-2-butynyloxy)pyrimidine

HRID 1592290Notes

Reaction equation

HRID 1592290 reaction equation
[H-].[Na+].[CH3:3][CH:4]([OH:8])[C:5]#[C:6][CH3:7].[Cl:9][C:10]1[CH:15]=[C:14](Cl)[N:13]=[CH:12][N:11]=1.[Cl-].[NH4+]>O1CCCC1>[Cl:9][C:10]1[CH:15]=[C:14]([O:8][CH:4]([CH3:3])[C:5]#[C:6][CH3:7])[N:13]=[CH:12][N:11]=1

Participants

6

Reactant 4

HCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 709434,6-DichloropyrimidineHCID 1413443-Pentyn-2-ol

Product 1

HCID 225996704-Chloro-6-(1-methyl-2-butynyloxy)pyrimidineYield 90.9%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent3×

Procedure

In 1 ml of tetrahydrofuran was suspended 0.04 g of sodium hydride (60% in oil), to which 0.5 ml of a tetrahydrofuran solution containing 0.06 g of 3-pentyn-2-ol was slowly added dropwise with stirring at room temperature. The mixture was stirred at room temperature for 20 minutes and then cooled to 0° C., to which 0.5 ml of a tetrahydrofuran solution containing 0.1 g of 4,6-dichloropyrimidine was slowly added dropwise, followed by further stirring for 30 minutes. The reaction mixture was then poured into a saturated aqueous ammonium chloride solution and extracted three times with t-butyl methyl ether. The organic layers were combined, washed with brine, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 0.12 g of 4-chloro-6-(1-methyl-2-butynyloxy)pyrimidine.

Workup

  1. additionwas slowly added dropwise
  2. stirringThe mixture was stirred at room temperature for 20 minutes
  3. additionwas slowly added dropwise
  4. stirringby further stirring for 30 minutes
  5. extractionextracted three times with t-butyl methyl ether
  6. washwashed with brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-d95ff7551a8c45568fca498aba6a8321
Source dataset
uspto-grants-2007_11
Patent number
US07291730B2

Reaction notes

Loading…