Hydrochloric Acid → 7-methoxy-1-oxo-1H-2-benzothiopyran-3-carboxylic acid
Reaction equation
[C:1]([C:4]1[CH:17]=[C:16]([O:18][CH3:19])[CH:15]=[CH:14][C:5]=1[CH:6]=[C:7]1[S:11]C(=S)N[C:8]1=[O:13])([OH:3])=O.[OH-:20].[Na+].Cl>>[CH3:19][O:18][C:16]1[CH:15]=[CH:14][C:5]2[CH:6]=[C:7]([C:8]([OH:20])=[O:13])[S:11][C:1](=[O:3])[C:4]=2[CH:17]=1Participants
4
Procedure
A solution of the benzylidenerhodanine of Example 7 in 18 ml. of 15% NaOH is refluxed for 0.75 hour and poured into dilute HCl, whereupon a yellow solid forms. The solid is collected and recrystallized from ethanol to give 7-methoxy-1-oxo-1H-2-benzothiopyran-3-carboxylic acid as pale yellow needles, m.p. 291°-292°.
Workup
- customThe solid is collected
- customrecrystallized from ethanol
Sources & evidence
- ORD record
- ord-d1a0b4f9bff84331bceb8e46ba109ef0
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03960892
Reaction notes
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