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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694570Generated: October 27, 2026

2,2,6,6-Tetramethylpiperidine → HCID 67280685, compound

https://huagongshe.com/reaction/1694570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
Reactant3-Chloro-2-fluoropyridine-4-carboxylic acidHCID 12175428—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 67280685HCID 6728068549.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

At −60° C., n-butyllithium (1.50 M hexane solution) (75.9 mL) was dropwise added to tetrahydrofuran (100 mL) solution of 2,2,6,6-tetramethylpiperidine (12.5 g), and stirred at −78° C. for 30 minutes. At −78° C., 3-chloro-2-fluoroisonicotinic acid (5.00 g) was added to the reaction liquid, and stirred at −78° C. for 2 hours. Then, at −78° C., tetrahydrofuran (50 mL) solution of 1,4-dioxaspiro[4.5]decan-8-one (5.78 g) was added to the reaction liquid, and stirred for 30 minutes at −78° C. The reaction liquid was warmed up under cooling with ice, and water and hexane were added thereto in that order. The aqueous layer and the organic layer were separated from each other, then the aqueous layer was made acidic (pH of 1 to 2) with 2 M hydrochloric acid added thereto and the stirred at room temperature for 2 hours. The formed solid was taken out through filtration, washed with water, and dried under reduced pressure to obtain the entitled compound (4.39 g, 49%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158791B2
Source datasetuspto-grants-2012_04
ORD IDord-3a148249187a437c925d028af8785908
Source noteuspto-grants-2012_04