Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Furaldehyde | HCID 10351 | — |
| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178418471 | HCID 178418471 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 19885922 | HCID 19885922 | — |
Reaction Steps
To a stirred solution of 3-phenylpropyl magnesium bromide (4.5 ml of a 2.73M solution in ethyl ether, 12.3 mmol, generated from 1-bromo-3-phenylpropane and magnesium and initiated with iodine) at 0° under argon, was added dropwise 3-furaldehyde (1.08 g., 11.2 mmol) in 5 ml ethyl ether. This solution was allowed to warm to room temperature, stirred for 20 minutes, and then poured over crushed ice containing several drops of concentrated sulfuric acid. The resulting mixture was partitioned between ethyl ether and 5% sodium bisulfite. The organic portion was washed with 5% sodium bicarbonate solution, water, saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to give an oil. This material was further purified by flash chromatography (silica, 20% ethyl acetate/hexane) to give the desired alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05134128 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-078415d80342456ab2945148936f90e0 |
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| Source note | uspto-grants-1992_07 |
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