Imidazole → 1-t-BUTYLDIMETHYLSILYLOXY-2,3-DIMERCAPTOPROPANE

HRID 365774

Reaction equation

HRID 365774 reaction equation
[SH:1][CH:2]([CH2:5][SH:6])[CH2:3][OH:4].N1C=CN=C1.[Si:12](Cl)([C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:14])[CH3:13].[Cl-].[NH4+]>C1COCC1>[Si:12]([O:4][CH2:3][CH:2]([SH:1])[CH2:5][SH:6])([C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:14])[CH3:13]

Participants

6

Conditions

Temperature
0 °C

Procedure

To a solution of 2,3-dimercapto-1-propanol (15.0 ml, 150 mmol) and imidazole (15.3 g, 224 mmol, 1.5 eq) in THF (300 mL) was added t-butyldimethylsilyl chloride (21.4 g, 142 mmol, 0.95 eq) at 0° C. The mixture was stirred at 0° C. for 1 hr and at room temperature for 18 hr. A saturated solution of ammonium chloride was added and the aqueous phase was extracted with dichloromethane. The organic layer was dried with anhydrous sodium sulphate and the solvent was evaporated under reduced pressure. The crude material was purified by flash chromatography with a mixture of hexane and ethyl acetate (90:10) to give the pure compound (32.04 g) in 94.5% yield.

Workup

  1. extractionthe aqueous phase was extracted with dichloromethane
  2. dry with materialThe organic layer was dried with anhydrous sodium sulphate
  3. customthe solvent was evaporated under reduced pressure
  4. customThe crude material was purified by flash chromatography with a mixture of hexane and ethyl acetate (90:10)

Sources & evidence

ORD record
ord-3d95563d7f794485bd6c0790606e1b60
Source dataset
uspto-grants-2000_10
Patent number
US06127540

Linked notes

Loading…