Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 579418 | HCID 579418 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 14500545 | HCID 14500545 | — |
Reaction Steps
Ten grams of N-(2,6-dimethylphenyl)-4-fluorobenzamide were dissolved in 50 ml of dimethylsulfoxide in a high pressure/temperature bomb. Anhydrous dimethylamine (18.5 g) was added and the reaction vessel sealed and heated at 150° C. for 18 hours. The bomb was cooled and the contents poured into water. The mixture was extracted with chloroform. The organic layer was washed with water and a saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated in vacuo. The resulting residue was crystallized from methanol/water affording the desired title product in yield, m.p. 215-217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04981866 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-00b140566df14e81b20ae6b5ec8c41e9 |
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| Source note | uspto-grants-1991_01 |
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