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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063368Generated: November 2, 2026

Potassium bisulfate → tert-Butyl 4-formylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1063368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bisulfateHCID 516920—
Reactanttert-Butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylateHCID 11065582—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430108%

Reaction Steps

A solution of 5.46 g (143.8 mmol) of LAH in 600 ml THF was cooled (−50° C.) and treated during 25 min with a solution of 35.6 g (130.7 mmol) of 4-(Methoxy-methyl-carbamoyl)-piperidine-1-carboxylic acid tert-butyl ester in 600 ml THF. The reaction was warmed up to RT for 3.5 h, cooled (−78° C.) and hydrolyzed with a suspension of 35 g MgSO4.7H2O, 35 g silicagel in 130 ml aqueous 10% KHSO4. The cooling bath was removed, THF was added, the mixture was stirred for 30 min and filtered. After evaporation, the residue was dissolved in CH2Cl2, dried (Na2SO4) and evaporated to give 30.1 g (quantitative) of 4-Formyl-piperidine-1-carboxylic acid tert-butyl ester, MS: 213 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964974B2
Source datasetuspto-grants-2005_11
ORD IDord-f4fd6cf886844fe1ba60134930b60649
Source noteuspto-grants-2005_11