HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanopyridine → HCID 178426512, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanopyridine | HCID 7506 | — |
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Product | HCID 178426512 | HCID 178426512 | 72.5% |
Reaction Steps
The title compound was prepared from 4-cyanopyridine (9.72 g, 93 mmol) and 4-methylaniline (10 g, 93 mmol) by following the procedure described in preparation 10 (14.3 g, yield 72.5%, mp 120-123° C., purity 98.75% by HPLC). 1H-NMR (CDCl3):δ 2.33 (s, 3H), 5.06 (bs, 2H, D2O exchangeable), 6.84-6.86 (d, 2H), 7.16-7.18 (d, 2H), 7.71-7.72 (d, 2H), 8.66-8.67 (d, 2H). IR (KBr) cm−1: 3437, 3138, 1644. MS m/z:212.1 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365069B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-816b45313137411c94a9b922be78d8d1 |
| Source note | uspto-grants-2008_04 |