Ethyl Thioglycolate → HCID 54284218, compound
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[CH:10]([C:11]2[CH:16]=[C:15]([N+:17]([O-:19])=[O:18])[CH:14]=[CH:13][C:12]=2Cl)[C:9]([C:21]([O:23][CH3:24])=[O:22])=[C:8]([CH3:25])[N:7]([CH3:26])[C:6]=1[CH3:27])=[O:4].[Na].[CH2:29]([O:31][C:32](=[O:35])[CH2:33][SH:34])[CH3:30]>CCOCC>[CH3:1][O:2][C:3]([C:5]1[CH:10]([C:11]2[CH:16]=[C:15]([N+:17]([O-:19])=[O:18])[CH:14]=[CH:13][C:12]=2[S:34][CH2:33][C:32]([O:31][CH2:29][CH3:30])=[O:35])[C:9]([C:21]([O:23][CH3:24])=[O:22])=[C:8]([CH3:25])[N:7]([CH3:26])[C:6]=1[CH3:27])=[O:4]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 19.7 g of 1,2,6-trimethyl-(2-chloro-5-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid dimethyl ester (melting point 190°C) in 200 ml of alcohol is heated to reflux and 60 ml of a solution of 2.3 g of sodium in 100 ml of alcohol, together with 13.2 g of mercaptoacetic acid ethyl ester, are added thereto. The mixture is refluxed for 15 hours and thereafter filtered and evaporated. The precipitate obtained after adding a little ether is recrystallized from methanol to yield yellow crystals of melting point 118°C.
Workup
- temperatureto reflux
- temperatureThe mixture is refluxed for 15 hours
- filtrationfiltered
- customevaporated
- customThe precipitate obtained
- customis recrystallized from methanol
- customto yield yellow crystals of melting point 118°C.
Sources & evidence
- ORD record
- ord-e2fc64bb591340cfbaecf240dbb93dc8
- Source dataset
- uspto-grants-1976_07
- Patent number
- US03968117
Reaction notes
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