Toluene → HCID 13653524, compound
Reaction equation
[CH2:1]([NH:3][C:4](=O)[CH2:5][O:6][C:7]1[C:12]([Cl:13])=[CH:11][C:10]([Cl:14])=[CH:9][C:8]=1[Cl:15])[CH3:2].C1(C)C=CC=CC=1.CSC.B>CO>[Cl:13][C:12]1[CH:11]=[C:10]([Cl:14])[CH:9]=[C:8]([Cl:15])[C:7]=1[O:6][CH2:5][CH2:4][NH:3][CH2:1][CH3:2]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
N-ethyl-2,4,6-trichlorophenoxyacetamide, the product of Example 13, 10.5 gm, was added to 80 ml of toluene. 7.0 ml of borane methyl sulfide [BH3 (CH3)2S] (2 equivalents) was then slowly added to the system. The system was heated at approximately 60° C. for 18 hours at which time reaction completion was checked by IR spectroscopy. 50 ml of methanol was then slowly added to the system. After addition of the methanol, the system was acidified by bubbling in HCl gas. Afterwards, the system was refluxed for 1 hour. The solvent was removed by stripping. The resulting oil was dissolved in methanol which was then stripped. The oil was next dissolved in methylene chloride and the methylene chloride solution was washed with a sodium hydroxide solution and then with water. The methylene chloride was removed by stripping to give 10.0 gm of the N-ethyl ethanolamine 2,4,6-trichlorophenylether.
Workup
- customby bubbling in HCl gas
- temperatureAfterwards, the system was refluxed for 1 hour
- customThe solvent was removed by stripping
- dissolutionThe resulting oil was dissolved in methanol which
- dissolutionThe oil was next dissolved in methylene chloride
- washthe methylene chloride solution was washed with a sodium hydroxide solution
- customThe methylene chloride was removed
Sources & evidence
- ORD record
- ord-8627f7b177434129a8aed71ddd3aeedd
- Source dataset
- uspto-grants-1986_05
- Patent number
- US04588735
Reaction notes
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