Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Methionin AL | HCID 446793 | — |
| Reactant | (4-Bromobutyl)triphenylphosphanium bromide | HCID 2733851 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 10977131 | HCID 10977131 | — |
Reaction Steps
Metal sodium (303 mg) was added to dry 2-propanol (30 mL), and the mixture was stirred at 70° C. After the sodium was dissolved, benzaldehyde (1.0 g) was added to the solution at 0° C., 4-bromobutyltriphenylphosphonium bromide (5.4 g) was then added, and the mixture was gradually warmed to room temperature. After 5 hours, the reaction mixture was concentrated under reduced pressure, ethyl acetate was added to the residue, and the resultant mixture was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was then purified by column chromatography on silica gel (hexane) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552188B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-9d2367d9d44b456fac0bc0d0bb752681 |
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| Source note | uspto-grants-2003_04 |
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