HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 13290240, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chloro-N-ethylbenzenamine | HCID 587841 | — |
| Reactant | 2,4,6-Trichloro-5-pyrimidinecarboxaldehyde | HCID 10932746 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13290240 | HCID 13290240 | 72.3% |
Reaction Steps
Solutions of 15.56 g (0.1 mole) of 4-chloro-N-ethylaniline (III) and 11.13 g (0.11 mole) of triethylamine, in each case in 50 ml of tetrahydrofuran, were successively added dropwise to a solution of 21.14 g (0.1 mole) of 2,4,6-trichloropyrimidine-5-carbaldehyde (II) in 100 ml of tetrahydrofuran. The solution was then stirred for three hours at room temperature and the triethylammoniumchloride was filtered off. The filtrate was then evaporated in vacuo and stirred with 150 ml of methanol at 0° C. 23.9 g of colorless crystals were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04619885 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-72367fbf2f7d43a9a7dcdb485971a387 |
| Source note | uspto-grants-1986_10 |