HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416545Generated: November 1, 2026
N-Methyl dicyclohexylamine → HCID 69922546, compound
https://huagongshe.com/reaction/2416545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methyl dicyclohexylamine | HCID 24210 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Ethyl trans-crotonate | HCID 429065 | — |
| Reactant | 4-(Pyrimidin-2-yl)bromobenzene | HCID 22287544 | — |
| Catalyst | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69922546 | HCID 69922546 | 70% |
Reaction Steps
Dioxane (2 mL) was added to a mixture of 2-(4-bromophenyl)pyrimidine (0.59 g, 2.51 mmol, prepared as described in U.S. Pat. No. 5,780,473), tri-t-butylphosphonium tetrafluoroborate (36 mg, 0.12 mmol), and tris(dibenzylideneacetone)dipalladium(0) (57 mg, 0.062 mmol). N-Methyldicyclohexylamine (0.64 mL, 2.99 mmol) and ethyl crotonate (0.62 mL, 4.99 mmol) were added and the mixture was stirred for 18 h at room temperature. The mixture was diluted with ethyl acetate, filtered through a small plug of silica gel which was washed with additional ethyl acetate, and the combined filtrates were concentrated. Purification by chromatography (SiO2, 5:1 hexane/ethyl acetate) provided 0.47 g (70%) of the title compound as an off-white solid. MS 269 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825170B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-1d8cf2c969e04f8c849c3abb06db7d3e |
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| Source note | uspto-grants-2004_11 |
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