HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 20438894, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Phenyl-3-isopropyl-5-hydroxymethyloxazolidine | HCID 12566198 | — |
| Reactant | HCID 20438889 | HCID 20438889 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20438894 | HCID 20438894 | 41.6% |
Reaction Steps
22.2 g of 2-phenyl-3-isopropyl-5-hydroxymethyloxazolidine was dissolved in 130 ml of anhydrous dimethyl formamide, and with stirring, 50% sodium hydride was added. To the resulting solution was added a solution of 22.75 g of 2-chloro-6-(tetrahydro-2-pyranyloxy)methylpyridine in 250 ml of anhydrous dimethyl formamide. The mixture was stirred at 80° C. for 1 hour. After the reaction, the solvent was distilled off under reduced pressure, and 500 ml of 10% hydrochloric acid was added. The mixture was stirred at 80° C. for 20 minutes. The reaction solution was evaporated to dryness under reduced pressure to afford 10 g (yield 41.6%) of 1-isopropylamino-3-(6-hydroxymethyl-2-pyridyloxy)-2-propanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04482562 |
| Source dataset | uspto-grants-1984_11 |
| ORD ID | ord-23e76a825c5b4e2f831e664b1ed01282 |
| Source note | uspto-grants-1984_11 |