참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Imidazole | HCID 795 | — |
| 반응물 | Iodine | HCID 807 | — |
| 반응물 | Triphenylphosphane dichloride | HCID 13797396 | — |
| 반응물 | Tert-butyl [1-(4-fluorophenyl)-2-hydroxyethyl]carbamate | HCID 58200246 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | [1-(4-Fluoro-phenyl)-2-iodo-ethyl]-carbamic acid tert-butyl ester | HCID 58200314 | 58% |
반응 단계
To a room temperature solution of triphenylphosphine dichloride (1.53 g (5.85 mmol) in methylene chloride was added iodine (1.481 g, 5.85 mmol). The mixture was stirred for fifteen minutes, then imidazole (663 mg, 9.74 mmol) was added. The mixture was stirred another 15 minutes, then [1-(4-fluoro-phenyl)-2-hydroxy-ethyl]carbamic acid tert-butyl ester (1.0 g, 3.9 mmol) was added. The mixture was heated to reflux for two hours, then stirred at room temperature overnight. Solvent was removed under reduced pressure, and the residue was partitioned between ethyl acetate and saturated aqueous sodium thiosulfate. The organic layer was separated, washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was chromatographed through silica (5-10% ethyl acetate/hexanes) to give 820 mg (58%) of [1-(4-fluoro-phenyl)-2-iodo-ethyl]-carbamic acid tert-butyl ester, MP=138-139° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08871760B2 |
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| 출처 데이터셋 | uspto-grants-2014_10 |
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| ORD ID | ord-4d1d6fe8d4b04a86b69a86abb67c3011 |
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| 출처 메모 | uspto-grants-2014_10 |
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