Lithium Hydroxide → HCID 23453516, compound
Reaction equation
C([O:3][C:4](=[O:24])[CH:5]([CH2:17]C1C=CC=CC=1)[CH:6]([C:9]1([C:15]#[N:16])[S:14][CH2:13][CH2:12][CH2:11][S:10]1)[CH2:7][F:8])C.[OH-].[Li+]>C(O)C>[C:15]([C:9]1([CH:6]([CH2:7][F:8])[CH:5]([CH3:17])[C:4]([OH:24])=[O:3])[S:10][CH2:11][CH2:12][CH2:13][S:14]1)#[N:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 3 g of the ethyl ester of Example 22, paragraph 1, in 40 ml of ethanol is treated with 15 ml of a 1 M solution of lithium hydroxide for about 40 hours at 25° C. The mixture is then acidified and extracted well with chloroform. The organic phase is dried and concentrated to afford the title compound.
Workup
- extractionextracted well with chloroform
- customThe organic phase is dried
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-a09998e1758c47558daa3de93d43fe5b
- Source dataset
- uspto-grants-1981_07
- Patent number
- US04277395
Reaction notes
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