HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-n-propylpyridine-3-carboxylate → Hydroxymethyl-2-n-propylpyridin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-n-propylpyridine-3-carboxylate | HCID 18706942 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | Hydroxymethyl-2-n-propylpyridin | HCID 18707030 | 90% |
Reaction Steps
Ethyl 2-n-propylpyridine-3-carboxylate was reduced with lithium aluminum hydride by the general synthetic principle outlined in example 1, step 4, to afford 3 hydroxymethyl-2-n-propylpyridin as a yellow oil in 90% yield. 1H--NMR (CDCl3, 200 MHz) δ: 0.98 (t, 3 H); 1.72 (sextet, 2 H); 2.75 (t, 2 H); 3.35 (br s, 1 H); 4.74 (s, 2 H); 7.12 (dd, 1 H); 7.74 (dd, 1 H); 8.39 (dd, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06080754 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-2dc2e6711def4f74a95f0885e916d2e2 |
| Source note | uspto-grants-2000_06 |