HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(1,1-Dimethylethyl)-2-phenyloxazolidine-5-methanol → HCID 21388034, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(1,1-Dimethylethyl)-2-phenyloxazolidine-5-methanol | HCID 108810 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 21388031 | HCID 21388031 | — |
| Reactant | 1,7-Dichloro-3-methylisoquinoline | HCID 21388033 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 21388034 | HCID 21388034 | — |
Reaction Steps
0.74 g of Potassium is dissolved in 15 ml of absolute tert.-butanol and 4.0 g of 1,7-dichloro-4-methylisoquinoline [m.p. 90°-92°: preparable in manner analogous to that described in Helv. Chim. Acta 52 (1969) 1755-1762 for the preparation of 1,7-dichloro-3-methylisoquinoline] and 4.4 g of 3-tert.-butyl-5-hydroxymethyl-2-phenyloxazolidine are added. The solution is heated to 50° for 1 hour, whereupon it is evaporated to dryness. The product is digested in water, extracted with ether, the ether phase dried and the ether distilled off. 1-(3-tert.-Butyl-2-phenyl-5-oxazolidinyl-methoxy)-7-chloro-4-methylisoquinoline is obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04067873 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-af7997618c58455197bca9e386e3403a |
| Source note | uspto-grants-1978_01 |