Hydrochloric Acid → HCID 21440743, compound
Reaction equation
[C:1]([C:4]1[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][C:5]=1[CH:6]=[C:7]1[S:11]C(=S)N[C:8]1=[O:13])([OH:3])=O.Cl.[OH-:21].[Na+]>>[CH3:19][O:18][C:15]1[CH:16]=[CH:17][C:4]2[C:1](=[O:3])[S:11][C:7]([C:8]([OH:21])=[O:13])=[CH:6][C:5]=2[CH:14]=1Participants
4
Procedure
A solution of the 5-(2-carboxy-5-methoxybenzylidene)rhodanine of Example 4 in dilute sodium hydroxide (35 ml. of 20% NaOH + 11 ml. H2O) is refluxed for one hour and then poured into dilute HCl. The resulting pale yellow solid is collected and recrystallized repeatedly from ethanol to give 6-methoxy-1-oxo-1H-2-benzothiopyran-3-carboxylic acid as pale yellow crystals, m.p. 278°-279°.
Workup
- customThe resulting pale yellow solid is collected
- customrecrystallized repeatedly from ethanol
Sources & evidence
- ORD record
- ord-f0d8ed6ea1b043c48fd30295b9a077c2
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04018891
Reaction notes
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