Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 1-(2,2-Diethoxyethoxy)-4-methoxybenzene | HCID 251315 | — |
| Reactant | p-tolylmethyl N-(pyrazine-2-carbonylamino)carbamate | HCID 478568 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methane | HCID 297 | — |
| Product | 2-(p-Methoxyphenoxy)-3-(dimethylamino)acrolein | HCID 54498024 | — |
Reaction Steps
Dry dimethylformamide (20 ml) was added dropwise to a stirred solution of phosphorus oxychloride (18 ml) maintained at a remperature of 0° C. The reaction mixture was allowed to warm to room temperature and p-methoxyphenoxyacetaldehyde diethyl acetal (16 g) was added with stirring. The mixture was cautiously heated with stirring to a temperature of 90° C. and then maintained at that temperature for 6 hr. The mixture was then cooled and poured slowly onto crushed ice (c. 1 kg) and the pH of the solution adjusted to pH10 by the addition, with stirring, of solid potassium carbonate. A benzene (95%)/alcohol (5%) solution (500 ml) was added to the reaction mixture and the total mixture heated just below its boiling point for 2 hr. The mixture was cooled, the organic layer was separated and dried, and the solvent removed by distillation under reduced pressure to give a black oil. The product crystallised from ethanol, after treatment with charcoal, to give 2-(p-methoxyphenoxy)-3-(dimethylamino)-acrolein (6.4 g) which was characterised by p.m.r. spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04248618 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-23981861004f46439e6b3bde4d86c737 |
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| Source note | uspto-grants-1981_02 |
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