HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2,4,6-trimethylpyrimidine-5-carboxylate → HCID 13934576, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2,4,6-trimethylpyrimidine-5-carboxylate | HCID 13203796 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13934576 | HCID 13934576 | — |
Reaction Steps
(a) Ethyl 2,4,6-trimethylpyrimidine-5-carboxylate [11.0 g; prepared according to Urban & Shnider, Helv. Chim Acta, 41, 1806 (1958)] was stirred with a slight excess of lithium aluminium hydride in dry tetrahydrofuran (100 ml) at room temperature for 2 hr. The solvent was evaporated and the residue was shaken with a little water. The dried (MgSO4) ethyl acetate extract was evaporated and the residue was purified by column chromotography over alumina with ethyl acetate elution to give 5-(hydroxymethyl)-2,4,6-trimethylpyrimidine as white crystals, mp 68° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04659362 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-60112536e4e041d688689ee815bf6656 |
| Source note | uspto-grants-1987_04 |