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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| Reactant | tert-Butyl 4-formyl-1H-imidazole-1-carboxylate | HCID 15480636 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | tert-butyl 4-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]imidazole-1-carboxylate | HCID 90415189 | 72.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434719B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-ae39e1d0f11d487da6def10728774fec |
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| Source note | uspto-grants-2016_09 |
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