Potassium tert-butoxide → 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine

HRID 1721045Notes

Reaction equation

HRID 1721045 reaction equation
[CH2:1]([O:3][C:4]([N:6]=[C:7]1[N:11]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:21])([F:20])[F:19])[CH:13]=2)[CH2:10][CH:9]([CH2:22]Br)[S:8]1)=[O:5])[CH3:2].CC(C)([O-])C.[K+]>C(O)(C)(C)C>[CH2:1]([O:3][C:4]([N:6]=[C:7]1[N:11]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:20])([F:21])[F:19])[CH:13]=2)[CH2:10][C:9](=[CH2:22])[S:8]1)=[O:5])[CH3:2]

Participants

4

Reactant 2

HCID 23665647Potassium tert-butoxideHCID 536349452-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromomethylthiazolidine

Product 1

HCID 540384642-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidineYield 44.5%

Reagents, catalysts & solvents 1

HCID 6386tert-ButanolSolvent

Procedure

A solution of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromomethylthiazolidine (0.7 g) and potassium t-butoxide (0.25 g) in t-butanol (30 ml) was refluxed for 5 hours, and the solvent was distilled off under reduced pressure. The residue was extracted with chloroform (100 ml), washed with water and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was subjected to column chromatography to give 0.25 g of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine (Compound (i)).

Workup

  1. distillationthe solvent was distilled off under reduced pressure
  2. extractionThe residue was extracted with chloroform (100 ml)
  3. washwashed with water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customAfter removal of the solvent

Sources & evidence

ORD record
ord-1eb03a7d3ee645f1b83695f64b78b2da
Source dataset
uspto-grants-1996_04
Patent number
US05508415

Reaction notes

Loading…