Reaction equation
Cl[C:2]([O:4][C:5]1[CH:10]=[C:9]([Cl:11])[C:8]([Cl:12])=[CH:7][C:6]=1[Cl:13])=[O:3].[C:14]([OH:18])([CH3:17])([CH3:16])[CH3:15].N1C2C(=CC=CC=2)C=CC=1>C(Cl)Cl>[C:2](=[O:3])([O:4][C:5]1[CH:10]=[C:9]([Cl:11])[C:8]([Cl:12])=[CH:7][C:6]=1[Cl:13])[O:18][C:14]([CH3:17])([CH3:16])[CH3:15]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
T-Butyl 2,4,5-trichlorophenyl carbonate is a known compound and one method for its preparation is described in an article by W. Broadbent, J. S. Morley and B. E. Stone in the Journal of the Chemical Society (C), 1967 pages 2632-2637. Briefly, in this method a solution of phosgene in toluene is treated with 2,4,5-trichlorophenol at -10° C, followed by addition of dimethylaniline at such a rate that the reaction temperature is maintained at 5°-10° C. The mixture is heated to 20°-24° C and maintained at this temperature for 12 hours. The mixture is cooled by addition of ice and the suspension filtered. From the organic layer in the filtrate, 2,4,5-trichlorophenyl chloroformate is isolated. A solution of the crude 2,4,5-trichlorophenyl chloroformate in methylene chloride is reacted with a solution of t-butanol and quinoline in methylene chloride. The reaction mixture is maintained at 20°-24° C for 12 hours. The mixture is cooled by addition of ice and the suspension is filtered. From the organic layer in the filtrate t-butyl 2,4,5-trichlorophenyl carbonate is isolated.
Workup
- temperatureThe reaction mixture is maintained at 20°-24° C for 12 hours
- temperatureThe mixture is cooled by addition of ice
- filtrationthe suspension is filtered
Sources & evidence
- ORD record
- ord-7a878406cf214f479336e843ab2f5754
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03991205
Linked notes
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