Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Acetylmorpholine | HCID 15543 | — |
| Reactant | (4-Chlorophenyl)(3,4-dimethoxyphenyl)methanone | HCID 798751 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Dimethomorph | HCID 86298 | — |
Reaction Steps
4-Chloro-3',4'-dimethoxy benzophenone (6.29 g, 25 mmol), sodium tert.-amylate (5.50 g, 50 mmol), acetyl morpholine (23.90 g, 185 mmol), and anhydrous toluene (50 ml) were stirred under reflux for 8 hours. After cooling, the solution was washed twice with water, dried, and the toluene distilled off on a rotary evaporator. The viscous residue was stirred at 50° C. with diisopropyl ether (40 ml), whereupon the substance solidified. After it had cooled to room temperature, the crude product was crushed, filtered by suction, washed with diisopropyl ether (2×5 ml) and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04920222 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-ba156369ae764f25ac4f0d56e1146947 |
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| Source note | uspto-grants-1990_04 |
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