Potassium Carbonate → HCID 86615225, compound

HRID 1183120Notes

Reaction equation

HRID 1183120 reaction equation
[CH3:1][O:2][C:3](=[O:6])[CH2:4][SH:5].C(=O)([O-])[O-].[K+].[K+].[C:13]([O:17][C:18](=[O:21])[CH2:19]Br)([CH3:16])([CH3:15])[CH3:14]>CN(C)C=O>[C:13]([O:17][C:18](=[O:21])[CH2:19][S:5][CH2:4][C:3]([O:2][CH3:1])=[O:6])([CH3:16])([CH3:15])[CH3:14]

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 16907Methyl ThioglycolateHCID 79177tert-Butyl bromoacetate

Product 1

HCID 86615225HCID 86615225, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

To a solution of mercapto-acetic acid methyl ester (1.0 g, 9.42 mmol) in dimethylformamide (10 mL) at room temperature was added potassium carbonate (1.69 g) followed by bromo-acetic acid tert-butyl ester (1.84 g, 9.42 mmol). The resulting suspension was stirred at ambient temperature overnight and then diluted with hexanes. The organic layer was washed with water three times and brine once, dried over sodium sulfate, filtered and concentrated to give a colorless oil, which was used directly in next step without purification. 1H NMR (CDCl3, 300 MHz) δ (ppm): 3.72 (s, 3H), 3.37 (s, 2H), 3.27 (s, 2H), 1.45 (s, 9H).

Workup

  1. washThe organic layer was washed with water three times and brine once
  2. dry with materialdried over sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customto give a colorless oil, which
  6. customwas used directly in next step without purification

Sources & evidence

ORD record
ord-27768f9d44a2413f86bc5fd51d0e4809
Source dataset
uspto-grants-2014_03
Patent number
US08664242B2

Reaction notes

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