HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromopyridine-2-carbaldehyde → HCID 178442119, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromopyridine-2-carbaldehyde | HCID 2757009 | — |
| Reactant | 2,6-Di(pentan-3-yl)aniline | HCID 12092548 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178442119 | HCID 178442119 | — |
Reaction Steps
A mixture of 8.00 g (43 mmol) of 6-bromopyridine-2-carbaldehyde, 10.0 g (43 mmol) of 2,6-bis(1-ethylpropyl)aniline in 80 ml of ethanol was refluxed for 8 h. The obtained solution was evaporated to dryness and the residue was re-crystallized from 20 ml of methanol. Yield 11.2 g (65%) of yellow crystalline powder. Anal. calc. for C22H29BrN2: C, 65.83; H, 7.28; N, 6.98. Found: C, 66.01; H, 7.23; N, 6.90. 1H NMR (CDCl3): δ 8.21 (m, 1H, 5-H in Py), 8.15 (s, 1H, CH═N), 7.69 (m, 1H, 4-H in Py), 7.59 (m, 1H, 3-H in Py), 7.10 (m, 1H, 4-H in dipentylphenyl), 7.03-7.04 (m, 2H, 3, 5-H in dipentylphenyl), 2.48 (m, 2H, CHEt2), 1.54 (m, 8H, CH2Me), 0.74 (t, J=7.3 Hz, 12H, CH2Me).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321858B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-33ad3d2f10af4946900c1dfa3ebec12e |
| Source note | uspto-grants-2016_04 |