HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065023Generated: November 2, 2026
2,6-Dimethylaniline → HCID 12877376, compound
https://huagongshe.com/reaction/1065023
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dimethylaniline | HCID 6896 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Chloromethyl)pyrimidine | HCID 12877371 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12877376 | HCID 12877376 | 70.3% |
Reaction Steps
48.4 g (0.4 mol) of 2,6-dimethylaniline, 55.3 g (0.4 mol) of potassium carbonate and 0.2 g of potassium iodide were heated to 100° C. in 60 ml of dimethylformamide, and 25.7 g (0.2 mol) of 2-chloromethyl-pyrimidine were then added dropwise. The reaction mixture was subsequently stirred at 100° C. for 5 hours and then poured onto 500 g of ice. It was then extracted three times with 150 ml of methylene chloride each time. The combined organic phases were dried over sodium sulphate and concentrated in vacuo. The residue was distilled under a high vacuum. 30 g (70% of theory) of N-(pyrimidin-2-yl-methyl)-2,6-dimethylaniline were obtained as a colorless oil of boiling point 150° C./0.2 mm Hg. ##STR13##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04328029 |
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| Source dataset | uspto-grants-1982_05 |
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| ORD ID | ord-e8e9104a901f41069e118af771b11c6f |
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| Source note | uspto-grants-1982_05 |
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