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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986989Generated: October 28, 2026

Potassium Iodide → HCID 12082300, compound

https://huagongshe.com/reaction/986989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDabcoHCID 9237—
ReactantPotassium CarbonateHCID 11430—
ReactantPicolyl chloride hydrochlorideHCID 23392—
Reactant1-(1,1-Dimethylethyl) 3-ethyl 4-oxo-1,3-piperidinedicarboxylateHCID 6420876—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 12082300HCID 1208230065.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-oxo-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (10.34 g, 38.2 mmol) in DMF (40 mL) at about 0° C. was added picolyl chloride hydrochloride (5.7 g, 34.7 mmol), potassium carbonate (14.4 g, 104.1 mmol) and potassium iodide (5.76 g, 34.7 mmol). After stirring at about 0° C. for about 2 hours, the ice bath was removed and DABCO (973 mg, 8.68 mmol) was added. The reaction mixture was stirred for about 30 min. and poured into a mixture of water and IPE. The organic layer was separated and washed with saturated aqueous NaHCO3 and saturated aqueous NaCl, dried over Na2SO4 and concentrated in vacuo. The crude residue was crystallized from hexanes to give a white solid (8.19 g, yield 65%). 1H-NMR (CDCl3) δ 1.17 (t, 3H), 1.48 (s, 9H), 1.55 (s, 2H), 2.61 (m, 1H), 2.71 (m, 1H), 3.31-3.50 (m, 3H), 4.11 (d, 2H), 4.49 (d, 1H), 7.06 (br s, 1H), 7.17(d, 1H), 1H), 8.40 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630487B2
Source datasetuspto-grants-2003_10
ORD IDord-7bda91fce38d4d37ae7029c623ddf63b
Source noteuspto-grants-2003_10