Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57448생성일: 2026년 10월 24일
tert-Butylsulfinamide, (S)-(-)- → tert-butyl 4-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]imidazole-1-carboxylate
https://huagongshe.com/ko/reaction/57448
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| 반응물 | tert-Butyl 4-formyl-1H-imidazole-1-carboxylate | HCID 15480636 | — |
| 촉매 | Copper Sulfate | HCID 24462 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | tert-butyl 4-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]imidazole-1-carboxylate | HCID 90415189 | 72.8% |
반응 단계
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)+
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434719B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-ae39e1d0f11d487da6def10728774fec |
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| 출처 메모 | uspto-grants-2016_09 |
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