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Methyl 2-(2-sulfamoylphenyl)acetate → 2H-1,2-Benzothiazin-3(4H)-one

HRID 977899
Notes
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Reaction equation

HRID 977899 reaction equation
[S:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[CH2:11][C:12]([O:14]C)=O)(=O)(=O)[NH2:2]>[OH-].[Na+]>[S:1]1[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=2[CH2:11][C:12](=[O:14])[NH:2]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 13064551Methyl 2-(2-sulfamoylphenyl)acetate

Product 1

HCID 218736702H-1,2-Benzothiazin-3(4H)-oneYield 96.4%

Reagents, catalysts & solvents 1

HCID 14798Sodium HydroxideSolvent

Procedure

A solution of 18 g of 2-sulfamoylphenylacetic acid, methyl ester, in 125 g of 10% aqueous sodium hydroxide was stirred at room temperature for 4 hours. The mixture was filtered and the filtrate acidified by the addition of concentrated hydrochloric acid with ice-water cooling. The resulting precipitate was collected by filtration, washed with water, and dried to afford 12.5 g of 2H-1,2-benzothiazin-3(4H)-one, 1,1-dioxide as an off-white powder, m.p. 190°-195° C. NMR (CDCl3 /DMSO-d6): δ 11.3 (1H, br s, NH), 7.85 (1H, br d), 7.3-7.7 (3H, m) and 4.0 (2H, s).

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • filtrationThe mixture was filtered
  • additionthe filtrate acidified by the addition of concentrated hydrochloric acid with ice-water cooling
  • filtrationThe resulting precipitate was collected by filtration
  • washwashed with water
  • customdried
  • Sources & evidence

    ORD record
    ord-805e585820a148938edfd94e5c6a2d98
    Source dataset
    uspto-grants-1987_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04662931

    Reaction notes

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