Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | HCID 22998459 | HCID 22998459 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22998524 | HCID 22998524 | 94.8% |
Reaction Steps
n-BuLi (2.39M, 177 μl) was slowly added to a solution of (2-trimethylsilylethoxymethyl)-N-(3,4-dimethyl-5-isoxazolyl)thiophene-3-sulfonamide (156 mg, 0.38 mmol) in THF at -78° C. under nitrogen. The reaction was stirred at -78° C. for 45 min., then benzaldehyde (45 μl, 0.42 mmol) was added in one lot at -78° C. and the solution was allowed to come to room temperature. Stirring was continued for 1 hr. Purification was achieved by column chromatography using 10% ethyl acetate/hexanes to give 179 mg 2-[2-(trimethylsilyl)ethoxymethyl]-N-(3,4-dimethyl-5-isoxazolyl)-2-(α-hydroxybenzyl)thiophene-3-sulfonamide as a yellow viscous oil (90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05594021 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-ddae87565ab74200ac6b6aede231fd14 |
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| Source note | uspto-grants-1997_01 |
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