HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Pyridinecarboxaldehyde → N-(3-Hydroxymethylphenyl)-alpha-(2-pyridyl)nitrone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Reactant | N-(3-Hydroxymethylphenyl)hydroxylamine | HCID 20131568 | — |
| Product | N-(3-Hydroxymethylphenyl)-alpha-(2-pyridyl)nitrone | HCID 86742279 | 65% |
Reaction Steps
The reaction of hydroxylamine 91 (1.36 g, 10 mmol) with 2-pyridinecarboxaldehyde (63) (1.07 g, 10 mmol) afforded, after workup, a yellow oil. The crude product was purified by passing through a short column of silica gel with 20:1 ethyl acetate/methanol as the eluant then recrystallized from acetone/petroleum ether to obtain 1.48 g (6.5 mmol, 65%) of 95 as a yellow crystalline solid: mp 117°-119° C.; IR (CH2Cl2) 3610, 3340, 1580, 1550, 1390, 1090 cm-1 ; 1H NMR (CDCl3) δ 4.53 (t, J=5.8, 1H), 4.65 (d, J=5.6 Hz, 2H), 7.28-9.27 (m, 9H); 13C NMR (CDCl3) δ 63.86, 119.70, 120.37, 124.33, 124.91, 128.59, 129.31, 135.80, 137.25, 143.61, 148.62, 149.50, 149.84. Anal. Calcd for C13H12N2O2 : C, 68.42; H, 5.26. Found: C, 68.52; H, 5.30.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04758669 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-8b56cc09696f471e8f93a0f082a73098 |
| Source note | uspto-grants-1988_07 |