HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Benzenamine, 2,6-diethyl-N-methylene-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 2,6-Diethylaniline | HCID 11369 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzenamine, 2,6-diethyl-N-methylene- | HCID 93179 | — |
Reaction Steps
2,6-Diethylaniline (149.2 grams; 1.0 mole), paraformaldehyde (40 grams), a 25% solution of trimethylamine (1.7 grams) and heptane were charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser connected to a Dean-Stark trap. The reaction mixture was heated and the water formed removed by azeotropic distillation. When no more water could be removed, the reaction mixture was stripped of solvent and distilled to yield the desired product N-methylene-2,6-diethylaniline as a colorless oil having a boiling point of 65°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976471 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-a26446e271234d7e90fffaa1f747d90e |
| Source note | uspto-grants-1976_08 |