Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57448Generated: October 25, 2026

tert-Butylsulfinamide, (S)-(-)- → tert-butyl 4-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]imidazole-1-carboxylate

https://huagongshe.com/reaction/57448

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
Reactanttert-Butyl 4-formyl-1H-imidazole-1-carboxylateHCID 15480636—
CatalystCopper SulfateHCID 24462—
Solvent1,2-DichloroethaneHCID 11—
Producttert-butyl 4-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]imidazole-1-carboxylateHCID 9041518972.8%

Reaction Conditions

Temperature65 °C

Reaction Steps

To CuSO4 (24.28 g, 152 mmol) and tert-butyl 4-formyl-1H-imidazole-1-carboxylate (19.9 g, 101 mmol) in DCE (100 mL) was added (S)-2-methylpropane-2-sulfinamide (13.52 g, 112 mmol). The reaction was heated to 65° C. for 18 hours. The reaction mixture was then cooled to room temperature and filtered through a pad of celite. The pad was rinsed with DCM (200 mL) and the filtrated was concentrated. The residue was then run through a pad of silica gel with heptane/EtOAc (3:1) as eluent. The filtrate was concentrated to give crude (S,E)-tert-butyl 4-(((tert-butylsulfinyl)imino)methyl)-1H-imidazole-1-carboxylate (22 g). LCMS (B) m/z 300.2 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-ae39e1d0f11d487da6def10728774fec
Source noteuspto-grants-2016_09