HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyripropanol → HCID 19885998, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyripropanol | HCID 72922 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | Tributyl(iodomethyl)stannane | HCID 10862926 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19885998 | HCID 19885998 | — |
Reaction Steps
Potassium hydride (52 mg, 1.30 mmol) was added to a solution of 3-(2-pyridyl)propan-1-ol (161.8 mg, 1.18 mmol) in tetrahydrofuran (3 ml) at room temperature under argon. After 30 minutes, a solution of tributylstannylmethyl iodide (510 mg, 1.18 mmol) in tetrahydrofuran (0.5 ml) was added. After stirring was continued at room temperature for 9 days, the mixture was diluted with ether and washed thoroughly with water. Evaporation of the dried (magnesium sulphate) organic layer gave an oil, which was flash chromatographed on silica using 60% ethyl ether/hexane. Fractions with Rf of about 0.53 on evaporation gave the title ether as a bright yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05134128 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-e0f89602aa1449f88d4fe1f4f12d2ac0 |
| Source note | uspto-grants-1992_07 |