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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527009Generated: November 3, 2026

tert-Butyl 4-formylpiperidine-1-carboxylate → tert-butyl 4-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/1527009

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
SolventDichloromethaneHCID 6344—
Producttert-butyl 4-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]piperidine-1-carboxylateHCID 5808020365.2%

Reaction Steps

To a round bottomed flask charged with a magnetic stir bar was added (S)-2-methylpropane-2-sulfinamide (20.46 g, 169 mmol), tert-butyl 4-formylpiperidine-1-carboxylate (30 g, 141 mmol), DCM (300 mL), and Ti(OEt)4 (59.0 ml, 281 mmol). The solution was stirred at room temperature for 3 h before it was quenched with brine (80 mL). The solution was stirred for 30 minutes before filtering. The filter cake was washed with DCM and the filtrate was placed in a separatory funnel and washed with water. The organics layer was dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue solidified to the title compound (29 g, 92 mmol, 65.1% yield) m/z 217.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085583B2
Source datasetuspto-grants-2015_07
ORD IDord-1e7a0a21f37d47fb8b304e5368c9f62f
Source noteuspto-grants-2015_07