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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095067Generated: November 1, 2026

Potassium Carbonate → 4-(2-Formyl-4-iodo-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1095067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-IodosalicylaldehydeHCID 252612—
Reactant1-(tert-Butoxycarbonyl)-4-(p-toluenesulfonyloxy)piperidineHCID 15734713—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(2-Formyl-4-iodo-phenoxy)-piperidine-1-carboxylic acid tert-butyl esterHCID 5774327484%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-iodosalicylaldehyde (3 g, 12.1 mmol) (Aldrich) in N,N-dimethylformamide (20 mL) was added anhydrous K2CO3 (5 g, 36.3 mmol), and 4-(toluene-4-sulfonyloxy)-piperidine-1-carboxylic acid tert-butyl ester (5.4 g, 18.1 mmol, ASTATECH). The reaction mixture was heated at 60° C. for 18 h. The mixture was cooled to room temperature, diluted with ethyl acetate, washed with water. The organic layer was separated, the aqueous layer was extracted with ethyl acetate. The organic layers were combined, washed with water, brine, dried over MgSO4, and concentrated to give crude 4-(2-formyl-4-iodo-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester as a yellow oil (Yield 4.38 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134001B2
Source datasetuspto-grants-2012_03
ORD IDord-cc2c979b317247feb5c24eb3d60a086a
Source noteuspto-grants-2012_03