Methanol → HCID 136399287, compound
Reaction equation
[OH:1][C:2]1[C:10]([C:11]([CH3:14])([CH3:13])[CH3:12])=[CH:9][C:5]([C:6]([SH:8])=[S:7])=[CH:4][C:3]=1[C:15]([CH3:18])([CH3:17])[CH3:16].CO.[Zn:21]>[Pt].CCOCC>[OH:1][C:2]1[C:10]([C:11]([CH3:13])([CH3:12])[CH3:14])=[CH:9][C:5]([C:6]([S-:8])=[S:7])=[CH:4][C:3]=1[C:15]([CH3:18])([CH3:17])[CH3:16].[OH:1][C:2]1[C:10]([C:11]([CH3:13])([CH3:12])[CH3:14])=[CH:9][C:5]([C:6]([S-:8])=[S:7])=[CH:4][C:3]=1[C:15]([CH3:18])([CH3:17])[CH3:16].[Zn+2:21]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Zinc bis(4-hydroxy-3,5-di-tert.-butyl dithiobenzoate) was prepared as follows. The acid, 4-hydroxy-3,5-di-tert.-butyl dithiobenzoic acid (0.4 g) was dissolved in 15 ml. of methanol. Zinc wire (1.2 cm2) was made the anode and platinum wire (1.4 cm2) was made the cathode. The methanol/acid mixture was placed in a container housing the wire electrodes and 0.1 g of zinc metal was dissolved in 12 hours using 70 ma current and 12 volts. The resulting zinc bis(4-hydroxy-3,5-di-tert.-butyl dithiobenzoate) was isolated from ether solution.
Workup
- customZinc bis(4-hydroxy-3,5-di-tert.-butyl dithiobenzoate) was prepared
- dissolutionwas dissolved in 12 hours
Sources & evidence
- ORD record
- ord-6f0c45e1ae144ed9a9efe621ad9f9e4c
- Source dataset
- uspto-grants-1986_01
- Patent number
- US04566982
Reaction notes
Loading…