Hydrochloric Acid → 8-methoxy-1-oxo-1H-2-benzothiopyran-3-carboxylic acid
Reaction equation
[C:1]([C:4]1[C:17]([O:18][CH3:19])=[CH:16][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:17]1[C:4]2[C:1](=[O:3])[S:11][C:7]([C:8]([OH:20])=[O:13])=[CH:6][C:5]=2[CH:14]=[CH:15][CH:16]=1Participants
4
Procedure
A solution of the benzylidenerhodanine of Example 10 in 46 ml. of 15% NaOH is refluxed for 0.75 hour, cooled, and poured into dilute HCl. The resulting tan precipitate is collected and air-dried. Two recrystallizations from methanol (charcoal) give 8-methoxy-1-oxo-1H-2-benzothiopyran-3-carboxylic acid as a pale yellow solid, m.p. 275° (dec.).
Workup
- temperaturecooled
- customThe resulting tan precipitate is collected
- customair-dried
- customTwo recrystallizations from methanol (charcoal)
Sources & evidence
- ORD record
- ord-3bd26851e24f478c840da46cad7af5a4
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04018891
Reaction notes
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