Sodium Bicarbonate → HCID 86742046, compound
Reaction equation
[Cl:1][CH2:2][CH2:3][C:4]12[CH2:16][CH2:15][C:14](=[O:17])[CH:13]=[C:12]1[C:11]1[C:6](=[CH:7][C:8]([O:20][CH2:21][C:22]([OH:24])=[O:23])=[C:9]([Cl:19])[C:10]=1[Cl:18])[CH2:5]2.C(=O)(O)[O-].[Na+:29]>O>[Cl:1][CH2:2][CH2:3][C:4]12[CH2:16][CH2:15][C:14](=[O:17])[CH:13]=[C:12]1[C:11]1[C:6](=[CH:7][C:8]([O:20][CH2:21][C:22]([O-:24])=[O:23])=[C:9]([Cl:19])[C:10]=1[Cl:18])[CH2:5]2.[Na+:29]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
{[9a-(2-Chloroethyl)-5,6-dichloro-3-oxo-2,3,9,9a-tetrahydro-1H-fluoren-7-yl]oxy}acetic acid (500 mg) is dissolved by stirring and warming with 0.25N sodium bicarbonate solution (5.4 ml). The solution is diluted to 10 ml and sterilized by filtration. All the water that is used in the preparation is pyrogen-free. The concentration of the active agent in the final solution is 5%.
Workup
- additionThe solution is diluted to 10 ml and sterilized by filtration
Sources & evidence
- ORD record
- ord-62360fab674544839110f158219ceed7
- Source dataset
- uspto-grants-1988_03
- Patent number
- US04731471
Reaction notes
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