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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752227Generated: October 28, 2026

n-Butyl lithium → HCID 71254114, compound

https://huagongshe.com/reaction/1752227

Reaction equation

Participants

RoleNameHCIDCharge
Reactantn-Butyl lithiumHCID 61028—
Reactant3,6-dibromo-9-((oxiran-2-yl)methyl)-9H-carbazoleHCID 2775473—
ReactantM-MEO CF3-METHANESULFONANILIDEHCID 23274414—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 71254114HCID 71254114—

Reaction Conditions

Temperature90 °C

Reaction Steps

N-butyllithium (2.5 M in hexanes, 48 ml) was added dropwise to an ice-cooled solution of 1,1,1-trifluoro-N-(3-methoxyphenyl)methanesulfonamide (22.07 g, 86.5 mmol) in dry dioxane (145 ml) over a 40 minute period. The solution was then stirred at ambient temperature for 15 minutes before addition of 3,6-dibromo-9-(oxiran-2-ylmethyl)-9H-carbazole (25.05 g, 65.7 mmol) followed by heating at 90° C. for an hour. The reaction was cooled then diluted with 1.2 L ethyl acetate and washed several times with water and finally brine. The organic layer was dried over MgSO4, filtered and condensed to give an orange viscous mixture. The residue was dissolved in 150 ml of 60% methylene chloride/hexanes, then concentrated to yellow foam to which a further 150 ml of 60% methylene chloride/hexanes was added and stirred overnight. The mixture was filtered and washed several times with 60% methylene chloride/hexanes until the solid was white giving 20.1 g of 99%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162980B2
Source datasetuspto-grants-2015_10
ORD IDord-5b4128cec96f42fa80fefb146d212cbb
Source noteuspto-grants-2015_10