Sodium Hydroxide → HCID 20390079, compound
Reaction equation
[CH3:1][S:2][CH2:3][S:4][CH:5]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:6]([O:8]CSC)=[O:7].[OH-].[Na+]>C(O)C>[CH3:1][S:2][CH2:3][S:4][CH:5]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:6]([OH:8])=[O:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.9 gms. of DL-α-[[(methylthio)methyl]thio]benzene acetic acid, (methylthio)methyl ester are dissolved in 10 ml. of ethanol. 20 ml. of 1 N alcoholic sodium hydroxide solution are added and the mixture is permitted to stand overnight. This is then concentrated, the residue is dissolved in water, the aqueous solution is extracted once with ether, then acidificed and the oil is extracted with ether. After drying with magnesium sulfate and evaporating the solvent 1.8 gms. of DL-α-[[(methylthio)methyl]thio]benzeneacetic acid are obtained as an oil.
Workup
- concentrationThis is then concentrated
- dissolutionthe residue is dissolved in water
- extractionthe aqueous solution is extracted once with ether
- extractionthe oil is extracted with ether
- dry with materialAfter drying with magnesium sulfate
- customevaporating the solvent 1.8 gms
Sources & evidence
- ORD record
- ord-4c0050867aa14ece9576a0c6f81eaeab
- Source dataset
- uspto-grants-1979_10
- Patent number
- US04171435
Reaction notes
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