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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929375Generated: October 30, 2026

2,2,6,6-Tetramethylpiperidine → 6-Chloro-2-iodo-3-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/1929375

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant2-Chloro-4-iodo-5-(trifluoromethyl)pyridineHCID 2773791—
Reactant2-Chloro-3-iodo-5-(trifluoromethyl)pyridineHCID 10990462—
ReactantButyllithiumHCID 178418339—
CatalystIodineHCID 807—
SolventTetrahydrofuranHCID 8028—
Product6-Chloro-2-iodo-3-(trifluoromethyl)pyridineHCID 1122053696%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2,2,6,6-tetramethylpiperidine (4.277 g, 5.110 mL, 30.28 mmol) in THF (18.00 mL) cooled to −78° C. was added nBuLi in hexanes (11.72 mL of 2.5 M, 29.30 mmol). The solution was allowed to warm up to 0° C. and was stirred for 15 minutes at that temperature before cooling it again to −78° C. Iodine (12.40 mg, 2.515 μL, 0.04884 mmol) was added followed by a dropwise addition of a solution containing a mixture of 2-chloro-3-iodo-5-(trifluoromethyl)pyridine (2 g, 6.505 mmol) and 2-chloro-4-iodo-5-(trifluoromethyl)pyridine (4.000 g, 13.01 mmol) in THF (18.00 mL). The solution was stirred at −78° C. for 2 hours. The reaction mixture was partitioned between a 1M solution of HCl and ether. The organic extract was washed with a saturated solution of sodium bicarbonate and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography to afford the title compound as a pale yellow oil (1.92 g, 32% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188071B2
Source datasetuspto-grants-2012_05
ORD IDord-60689a2ed56a438f98189e6fc994be9d
Source noteuspto-grants-2012_05