Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | 2,6-Dimethylaniline | HCID 6896 | — |
| Reactant | N,N-Dimethylbenzylamine | HCID 7681 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10993945 | HCID 10993945 | 95.2% |
Reaction Steps
180 g (3 mols) of sodium sulphate and 3 ml of dimethylbenzylamine were added to 121 g (1 mol) of 2,6-dimethylaniline in 200 ml of methylene chloride. 88 g (2 mols) of acetaldehyde were added to the mixture at 0° C. The mixture was stirred at 0° C. for 4 hours and was filtered, and the filtrate was concentrated in vacuo at a maximum bath temperature of 20° C. 140 g (95.2% of theory) of N-ethylidene-2,6-dimethylaniline were obtained as a reddish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04599448 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-d87293a426fb47e29c5d424594c57256 |
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| Source note | uspto-grants-1986_07 |
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