Hydrochloric Acid → HCID 58508460, compound
Reaction equation
CO.[OH-].[Na+].C([O:8][C:9]1[C:33]([CH3:34])=[CH:32][CH:31]=[CH:30][C:10]=1[C:11]([NH:13][C:14]1[CH:23]=[C:22]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH:21]=[CH:20][C:15]=1[C:16]([O:18]C)=[O:17])=[O:12])(=O)C.Cl>O1CCOCC1>[OH:8][C:9]1[C:33]([CH3:34])=[CH:32][CH:31]=[CH:30][C:10]=1[C:11]([NH:13][C:14]1[CH:23]=[C:22]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH:21]=[CH:20][C:15]=1[C:16]([OH:18])=[O:17])=[O:12]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Methanol (2 mL), dioxane (4 mL), and a 2 mol/L aqueous solution of sodium hydroxide (0.77 mL) were added to the obtained methyl 2-(2-acetoxy-3-methylbenzamido)-4-phenylbenzoate (0.062 g), followed by stirring at room temperature for 7 hours. The reaction mixture was adjusted to a pH of 1.1 with 6 mol/L hydrochloric acid. The solid substance was collected by filtration to obtain 0.044 g of 2-(2-hydroxy-3-methylbenzamido)-4-phenylbenzoic acid as a white solid.
Workup
- filtrationThe solid substance was collected by filtration
Sources & evidence
- ORD record
- ord-910728d9e98d492e9e6f377cfa0cb0da
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08492582B2
Reaction notes
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