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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369086Generated: November 1, 2026

Hexane → 1-(2-Diethylaminoethyl)-4-trifluoromethyl-6-iodo-3-hydroxy-3-(2-trifluoromethylphenyl)oxindole

https://huagongshe.com/reaction/1369086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantBenzene, 1-bromo-2-(trifluoromethyl)-HCID 9806—
Reactant1-(2-Diethylaminoethyl)-4-trifluoromethyl-6-iodoisatinHCID 11026552—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Diethylaminoethyl)-4-trifluoromethyl-6-iodo-3-hydroxy-3-(2-trifluoromethylphenyl)oxindoleHCID 1851865221%

Reaction Steps

To a solution of 2-bromobenzotrifluoride (0.3 mL, 2.23 mmol) in THF (1.5 mL) was added dropwise 1.53 N BuLi in hexane (1.45 mL, 2.22 mmol) over 10 min at −78° C. and the mixture was stirred for 10 min. The resulting solution (1.2 mL, 0.82 mmol) was then added dropwise to the cooled solution of 1-(2-diethylaminoethyl)-4-trifluoromethyl-6-iodoisatin (352 mg, 0.8 mmol) in THF (4 mL) at −78° C. via a syringe. The mixture was allowed to warm to room temperature and stirred for 30 min. The reaction was quenched with aqueous NaHCO3. The mixture was extracted with ethyl acetate, dried over MgSO4, and concentrated. The residue was purified by silica gel column chromatography with 50:1 to 40:1 chloroform/methanol to give the title compound (96.3 mg, 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576656B1
Source datasetuspto-grants-2003_06
ORD IDord-b45bc991801a4aa0a5ab8d6175f73d6f
Source noteuspto-grants-2003_06