Potassium Carbonate → HCID 86627028, compound

HRID 1677860Notes

Reaction equation

HRID 1677860 reaction equation
[C:1]([O:5][C:6](=[O:9])[CH2:7]Br)([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].[Cl:16][C:17]1[CH:22]=[C:21]([C:23]2[CH:28]=[CH:27][C:26]([S:29]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)(=[O:31])=[O:30])=[CH:25][CH:24]=2)[C:20]([OH:38])=[CH:19][CH:18]=1>CN(C=O)C>[Cl:16][C:17]1[CH:18]=[CH:19][C:20]([O:38][CH2:7][C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:9])=[C:21]([C:23]2[CH:24]=[CH:25][C:26]([S:29]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)(=[O:31])=[O:30])=[CH:27][CH:28]=2)[CH:22]=1

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 79177tert-Butyl bromoacetateHCID 67240920HCID 67240920, compound

Product 1

HCID 86627028HCID 86627028, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

A flask was charged with tert-butylbromoacetate (0.42 ml), dry DMF (20 ml), potassium carbonate (0.36 g) and the product from example 1 step (ii) (0.9 g) and then stirred at room temperature overnight. The mixture was quenched in water and extracted with diethylether, dried (MgSO4) and concentrated under reduced pressure to give an oil. The oil was purified by chromatography on silica eluting with isohexane/diethylether 2:1 to give the sub-title compound as a colourless oil, yield 0.6 g.

Workup

  1. customThe mixture was quenched in water
  2. extractionextracted with diethylether
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated under reduced pressure
  5. customto give an oil
  6. customThe oil was purified by chromatography on silica eluting with isohexane/diethylether 2:1

Sources & evidence

ORD record
ord-9cad35bb58914a2f8813c1114127cdc7
Source dataset
uspto-grants-2011_08
Patent number
US08008350B2

Reaction notes

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