Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diphenylacetaldehyde | HCID 13696 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Product | HCID 15238027 | HCID 15238027 | — |
Reaction Steps
To a mixture of ethylmagnesium bromide (5.7 ml; 3.0 M/L in ether solution) and THF (40 ml) was added dropwise a solution of the compound prepared in reference example 30 (3.0 g) in THF (20 ml) over a 10 min period. The mixture was stirred for 2 h at room temperature. To the mixture was added a solution of diphenylacetaldehyde (2.94 g) in THF (10 ml). The mixture was stirred for 2 h. After quenched by addition of ammonium chloride, the mixture was extracted with ether. The extract was washed with water and a saturated aqueous solution of sodium chloride, successively, dried over anhydrous magnesium sulfate, and evaporated. To a solution of the residue in ether (50 ml) was added manganese (IV) oxide (2.7 g) at room temperature. The mixture was stirred for 2 h. The mixture was filtrated, and evaporated. The residue was purified by silica gel column chromatography (n-hexane: ethyl acetate=7:1) to give the title compound (2.41 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962439 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-a9e2e4f7c5c749ee9653e91fd1505dc5 |
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| Source note | uspto-grants-1999_10 |
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