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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476333Generated: November 1, 2026

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

https://huagongshe.com/reaction/1476333

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
CatalystTitanium tetraethoxideHCID 76524—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 4-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]piperidine-1-carboxylateHCID 5808020385.2%

Reaction Steps

A solution of (S)-2-methylpropane-2-sulfinamide (2.0 g, 16.50 mmol) in THF (8.0 ml) and titanium(IV) ethoxide (17.3 ml, 82.51 mmol) were added sequentially to a solution of tert-butyl 4-formylpiperidine-1-carboxylate (3.70 g, 17.33 mmol) in THF (8.0 ml). The resulting mixture was stirred at r.t for 2 hours. The reaction mixture was poured into ice/water and the suspension filtered. The filtrate was extracted with EtOAc and the organic layer was dried with MgSO4, filtered and the filtrate was concentrated under reduced pressure. The residue was dried under vacuum to provide the title compound (4.45 g, yield: 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018381B2
Source datasetuspto-grants-2015_04
ORD IDord-287135b3f683431087b87a36610e4443
Source noteuspto-grants-2015_04