1-Oxo-1H-isothiochromene-3-carboxylic acid → HCID 178526106, compound
Reaction equation
[O:1]=[C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[CH:5]=[C:4](C(O)=O)[S:3]1.[C:15](=O)([OH:17])[O-:16].[Na+:19]>O>[O:1]=[C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[CH:5]=[CH:4][SH:3]1[C:15]([O-:17])=[O:16].[Na+:19]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred suspension of 4.50 g. (21.8 mM) of the carboxylic acid of Example 2 in 200 ml. of distilled water is added 1.833 g. (21.82 mM) of sodium bicarbonate. The mixture is then stirred at 25°-35° for 2 hours, whereupon all the solids dissolve. The solution is frozen and freeze-dried to give sodium 1-oxo-1H-2-benzothiopyran-2-carboxylate as a pale yellow solid, m.p. >350°.
Workup
- additionTo a stirred suspension of 4.50 g
- dissolutiondissolve
- temperatureThe solution is frozen
- customfreeze-dried
Sources & evidence
- ORD record
- ord-8c990f6a004c48b5a5b06986e7fa16c7
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04018891
Reaction notes
Loading…