Lithium Hydroxide → HCID 14877951, compound
Reaction equation
[Li+].[OH-].[F:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]([C:22]2[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=2)=[C:11]([N:17]2[CH:21]=[N:20][N:19]=[N:18]2)[C:12]([O:14]CC)=[O:13])=[CH:6][CH:5]=1>C(O)C.O>[F:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]([C:22]2[CH:23]=[CH:24][C:25]([F:28])=[CH:26][CH:27]=2)=[C:11]([N:17]2[CH:21]=[N:20][N:19]=[N:18]2)[C:12]([OH:14])=[O:13])=[CH:6][CH:5]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The saponification was performed by the addition of 1.14 mL of 2.0 M LiOH solution to a solution of 0.27 g (0.76 mmole) of ethyl α-[bis(4-fluorophenyl)methylene]-1 H-tetrazole-1-acetate in 5 mL of 95% ethanol at room temperature. After two hours, the crude reaction mixture was diluted with water and washed with diethyl ether (20 mL×2). The free acid in the aqueous layer was regenerated by the addition of aqueous HCl then extracted with diethyl ether, dried and evaporated. The crude acid was dried under high vacuum for 48 hours before it was used in the next step.
Workup
- customthe crude reaction mixture
- washwashed with diethyl ether (20 mL×2)
- additionThe free acid in the aqueous layer was regenerated by the addition of aqueous HCl
- extractionthen extracted with diethyl ether
- customdried
- customevaporated
- dry with materialThe crude acid was dried under high vacuum for 48 hours before it
Sources & evidence
- ORD record
- ord-142487dfea294d7c9780b9355b47b5d6
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05070206
Reaction notes
Loading…