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HRID 57448作成日:2026年10月25日
tert-Butylsulfinamide, (S)-(-)- → tert-butyl 4-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]imidazole-1-carboxylate
https://huagongshe.com/reaction/57448
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| 反応物 | tert-Butyl 4-formyl-1H-imidazole-1-carboxylate | HCID 15480636 | — |
| 触媒 | Copper Sulfate | HCID 24462 | — |
| 溶媒 | 1,2-Dichloroethane | HCID 11 | — |
| 生成物 | tert-butyl 4-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]imidazole-1-carboxylate | HCID 90415189 | 72.8% |
反応手順
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)+
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09434719B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-ae39e1d0f11d487da6def10728774fec |
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| 出典メモ | uspto-grants-2016_09 |
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