Hydrochloric Acid → HCID 18930437, compound

HRID 1464683Notes

Reaction equation

HRID 1464683 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[NH:12][C:11]([C:13]([O:15]CC)=[O:14])=[CH:10][C:9]=2[S:18]([C:21]([F:26])([F:25])[CH:22]([F:24])[F:23])(=[O:20])=[O:19])=[CH:4][CH:3]=1.[OH-].[Na+].Cl>C(O)C.O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[NH:12][C:11]([C:13]([OH:15])=[O:14])=[CH:10][C:9]=2[S:18]([C:21]([F:26])([F:25])[CH:22]([F:23])[F:24])(=[O:19])=[O:20])=[CH:6][CH:7]=1

Participants

6

Procedure

A solution of ethyl 5-(p-chlorophenyl)-4-[(1,1,2,2-tetrafluoroethyl)sulfonyl]pyrrole-2-carboxylate (0.54 g, 0.0012 mol) in ethanol is treated under nitrogen with a solution of sodium hydroxide (0.26 g, 0.0065 mol) in water. The reaction mixture is refluxed for three hours, poured into ice-water, treated with hydrochloric acid and extracted with ethyl acetate. The combined organic extracts are washed with water and brine, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain the title product as a gum (0.6 g).

Workup

  1. temperatureThe reaction mixture is refluxed for three hours
  2. extractionextracted with ethyl acetate
  3. washThe combined organic extracts are washed with water and brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-c2c9621b01424b53b367b0e3ba88a5d6
Source dataset
uspto-grants-1994_04
Patent number
US05306827

Reaction notes

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