Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Bromobenzaldehyde | HCID 81129 | — |
| Reactant | HCID 178478191 | HCID 178478191 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12319462 | HCID 12319462 | — |
Reaction Steps
2-bromobenzaldehyde (1 ml) was dissolved in diethyl ether (20 ml) and cooled to −78° C. 4-chlorophenylmagnesium bromide (1M diethyl ether solution, 9 ml) was added thereto and the reaction mixture was stirred for one hour at the same temperature. Saturated ammonium chloride aqueous solution was added thereto and the water layer was extracted with ethyl acetate. The organic layer was dried with anhydrous magnesium sulfate. The solvent was distilled off and the obtained residue was purified by column chromatography to obtain the title compound (2.50 mg) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217701B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-a34926760fc345e4816783125743e392 |
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| Source note | uspto-grants-2007_05 |
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