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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234444Generated: October 30, 2026

Benzaldehyde → HCID 22998524, compound

https://huagongshe.com/reaction/234444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHCID 22998459HCID 22998459—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22998524HCID 2299852494.8%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594021
Source datasetuspto-grants-1997_01
ORD IDord-ddae87565ab74200ac6b6aede231fd14
Source noteuspto-grants-1997_01