HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Nitropyridine-2-carbaldehyde → HCID 10058503, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Nitropyridine-2-carbaldehyde | HCID 15145501 | — |
| Reactant | Dichloromethane ethylacetate | HCID 21226138 | — |
| Product | HCID 10058503 | HCID 10058503 | — |
Reaction Steps
2-(1,3-Dioxolanyl)-5-nitropyridine was prepared from 5-nitropyridine-2-carboxaldehyde by the procedure employed for the synthesis of Example III. Yield: 2.0 g (84%); mp 104°-105° C.; TLC Rf 0.73 (CH2Cl2 /EtOAc, 1:1, v/v); 1H NMR (90 MHz, CDCl3) δ 4.10 (s, 4H, CH2CH2), 5.92 (s, 1H, 2-CH), 7.72 (d, 1H, 3-H, J3,4 =8 Hz), 8.50 (dd, 1H, 4-H, J3,4 =8 Hz, J4,6 =2 Hz), 9.42 (d, 1H, 6-H, J4,6 =2 Hz). Anal. (C8 H8N2O4) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05721259 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-1af17961b2974db5a778f64806f53d45 |
| Source note | uspto-grants-1998_02 |