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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539619생성일: 2026년 10월 24일

Imidazole → [1-(4-Fluoro-phenyl)-2-iodo-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/539619

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물IodineHCID 807—
반응물Triphenylphosphane dichlorideHCID 13797396—
반응물Tert-butyl [1-(4-fluorophenyl)-2-hydroxyethyl]carbamateHCID 58200246—
용매DichloromethaneHCID 6344—
생성물[1-(4-Fluoro-phenyl)-2-iodo-ethyl]-carbamic acid tert-butyl esterHCID 5820031458%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871760B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-4d1d6fe8d4b04a86b69a86abb67c3011
출처 메모uspto-grants-2014_10