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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1066856생성일: 2026년 10월 27일

tert-Butyl N-(4-hydroxybutyl)carbamate → N-(t-butoxycarbonyl)-4-(2-fluoro-5-bromobenzyloxy)butylamine

https://huagongshe.com/reaction/1066856

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl N-(4-hydroxybutyl)carbamateHCID 545141—
반응물4-Bromo-2-(bromomethyl)-1-fluorobenzeneHCID 13553295—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물N-(t-butoxycarbonyl)-4-(2-fluoro-5-bromobenzyloxy)butylamineHCID 21196003—

반응 조건

온도-40 °C

반응 단계

In a 25 ml flask 4-(t-butoxycarbonylamino)butanol was dissolved in tetrahydrofuran (15 ml) under a nitrogen atmosphere. The solution was cooled to −40° C. and potassium tert-butoxide (1M in tetrahydrofuran, 2.14 ml, 2.14 mmol) was added slowly. The resulting mixture was stirred at −40° C. for thirty minutes. To this reaction mixture was added 2-fluoro-5-bromobenzyl bromide (521 mg, 1.94 mmol), added dropwise as a solution in tetrahydrofuran (3.5 ml). The resulting mixture was slowly warmed to 0° C. and stirred at this temperature for two hours. The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was partitioned between 1 M potassium carbonate and methylene chloride. The aqueous fraction was back-extracted with methylene chloride. The organic fractions were combined and dried over sodium sulfate. The solvents were removed in vacuo. The desired intermediate was further purified by liquid chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06245761B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-d3a78e57ef244b938203929a695e2ad2
출처 메모uspto-grants-2001_06