HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 3-Benzyloxybenzene-2-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methyl 3-(benzyloxy)benzoate | HCID 13368031 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Benzyloxybenzene-2-propanol | HCID 18973855 | 93% |
Reaction Steps
To a 0° solution of 2.2 mole of methyl magnesium iodide in 1.5 l. ether is added a solution of 200 g. (1.06 mole) of methyl 3-benzyloxybenzoate in 500 ml. ether and 500 ml. tetrahydrofuran. The reaction mixture is stirred for 3 hours and then added to 1.5 l. ice cold saturated ammonium chloride and 2 l. ether. The organic extract is dried over magnesium sulfate and evaporated to an oil. Crystallization of the crude oil in petroleum ether gives 186 g. (93%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04739079 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-4f3e509c72f04a328c0d519e9dfb6fc9 |
| Source note | uspto-grants-1988_04 |