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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | Benzene, 1-bromo-2-(trifluoromethyl)- | HCID 9806 | — |
| Reactant | 1-(2-Diethylaminoethyl)-4-trifluoromethyl-6-iodoisatin | HCID 11026552 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Diethylaminoethyl)-4-trifluoromethyl-6-iodo-3-hydroxy-3-(2-trifluoromethylphenyl)oxindole | HCID 18518652 | 21% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06576656B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-b45bc991801a4aa0a5ab8d6175f73d6f |
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| Source note | uspto-grants-2003_06 |
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