HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → (R)-(+)-1-Phenyl-1,3-propanediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium bis(2-methoxyethoxy)aluminiumhydride | HCID 21584525 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (R)-(+)-1-Phenyl-1,3-propanediol | HCID 2735120 | — |
Reaction Steps
To a solution of commercial (−)-(2S,3S)-2,3-epoxycinnamyl alcohol (10.0 mmol) in dimethoxyethane (50 mL) is added a 3.4 M solution of sodium bis(2-methoxyethoxy)aluminum hydride (Red-A1) in toluene (10.5 mmol) dropwise under nitrogen at 0° C. After stirring at room temperature for 3 h, the solution is diluted with ether and quenched with 5% HCl solution. After further stirring at room temperature for 30 min, the white precipitate formed is removed by filtration and boiled with ethyl acetate and filtered again. The combined organic extracts are dried with magnesium sulfate and concentrated to give (R)-3-phenyl-1,3-dihydroxypropane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07816345B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-3ca5729ff3fc4694b2075bb945241a3f |
| Source note | uspto-grants-2010_10 |