HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5-Ethoxypyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 5-Bromopyrimidine | HCID 78344 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | 5-Ethoxypyrimidine | HCID 19921688 | 25.6% |
Reaction Steps
Sodium (2.89 g. 125.8 mmol) was dissolved in ethanol (110 mL) and 5-bromopyrimidine (10.0 g, 62.9 mmol) added. The reaction was heated at 120° in an autoclave for 17 h and then allowed to stand at 23° for 60 h. The ethanol was removed under reduced pressure and water (5 mL) added to the concentrate. The aqueous phase was extracted with CH2Cl2 (4×100 mL). The combined organic extracts were washed with saturated NaCI solution, dried with anhydrous K2CO3, filtered, and concentrated under reduced pressure. Silica gel chromatography (Hexane/EtOAc; 70:30) of the concentrate yielded 5-ethoxypyrimidine (2.00 g, 25.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05300506 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-93fdb5b66b7b4670be73100e457367c7 |
| Source note | uspto-grants-1994_04 |