Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pentanamine | HCID 12019 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | 2-Methoxy-4,5-dimethyl-1,3-dinitrobenzene | HCID 11138818 | — |
| Product | Pendimethalin | HCID 38479 | 86.6% |
Reaction Steps
To a suitable reaction vessel equipment with a thermometer and mechanical stirrer was introduced 24 g 2,6-dinitro-3,4-dimethylanisole 94% (0.1 moles), 0.55 g CaCl2 (0.005 moles), and 43.5 g of (0.5 moles) 1-ethyl propylamine. The reaction mixture was stirred at a temperature of 25°-30° C. The progress of the reaction was followed by periodically withdrawing samples and analyzing for starting product and the new product formed. During 24 hours the starting product disappeared and the N-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitroaniline is gradually formed. After completion of the reaction as indicated by vapor phase chromatography, the excess of 1-ethyl-propylamine was recovered from the reaction mixture by distillation. The residue was dissolved in dichloromethane and the solution was successively washed with 5% aqueous hydrochloric acid, 5% aqueous sodium hydroxide and then by water to neutral and dried. The solvent is next recovered by distillation leaving an oily product which solidified. (25.2 g 96.6%) with a yield of 86.6 %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05475148 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-eac52a9c5abc4948b20f078e2ee5d921 |
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| Source note | uspto-grants-1995_12 |
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