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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Iodosalicylaldehyde | HCID 252612 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-4-(p-toluenesulfonyloxy)piperidine | HCID 15734713 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(2-Formyl-4-iodo-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester | HCID 57743274 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08134001B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-cc2c979b317247feb5c24eb3d60a086a |
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| Source note | uspto-grants-2012_03 |
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