Bromine → 2-(5-Bromo-1,3-thiazol-2-yl)propan-2-ol

HRID 351751Notes

Reaction equation

HRID 351751 reaction equation
[CH3:1][C:2]([C:13]1[S:14][CH:15]=[CH:16][N:17]=1)([O:4]COCC[Si](C)(C)C)[CH3:3].[Br:18]Br.C(=O)(O)[O-].[Na+]>C(Cl)(Cl)Cl>[Br:18][C:15]1[S:14][C:13]([C:2]([OH:4])([CH3:3])[CH3:1])=[N:17][CH:16]=1

Participants

5

Procedure

To a solution of 2-(1-methyl-1-{[2-(trimethylsilyl)ethoxy]methoxy}ethyl)thiazole from Step 2 in chloroform (2 mL mmol) at room temperature was added bromine (2 molar eq) and the resulting mixture was stirred for 1 hour. Solid sodium bicarbonate (0.55 eq) was added and the mixture was stirred for 5 hours. More sodium bicarbonate was added (0.55 eq) and stirring was continued for 18 hours. After a final addition of sodium bicarbonate (0.55 eq) the mixture was stirred for a further 5 hours, diluted with chloroform and the organic phase was washed with saturated aqueous sodium bicarbonate, then with water, dried and evaporated. The crude material was chromatographed, eluting with a 3:7 mixture of ethyl acetate and hexane to afford the desired product.

Workup

  1. stirringthe mixture was stirred for 5 hours
  2. stirringstirring
  3. waitwas continued for 18 hours
  4. stirringwas stirred for a further 5 hours
  5. washthe organic phase was washed with saturated aqueous sodium bicarbonate
  6. dry with materialwith water, dried
  7. customevaporated
  8. customThe crude material was chromatographed
  9. washeluting with a 3:7 mixture of ethyl acetate and hexane

Sources & evidence

ORD record
ord-df6ba86e611b4bdba81cf201b740623b
Source dataset
uspto-grants-2004_06
Patent number
US06743802B2

Reaction notes

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