Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | t-Butyl 7-phenyl-2-heptenoate | HCID 54541139 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18790170 | HCID 18790170 | — |
Reaction Steps
t-butyl 7-phenylhept-2-enoate (2 g; 7.7 mmol) and thiophenol (1.2 g; 11 mmol) are dissolved in THF (25 mL) and cooled to 0° C. n-BuLi (2.5 M in hexane; 0.3 mL; 0.7 mmol) is added dropwise and the reaction is allowed to warm and stir at 20° C. for 3 hours. The reaction is concentrated in vacuo and purified by column chromatography using 5% Et2O/petroleum ether to obtain t-butyl 7-phenyl-3-phenylsulfanylheptanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057369 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-9e54f8035b1d462ca88ebe87b2669bb2 |
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| Source note | uspto-grants-2000_05 |
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