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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12922생성일: 2026년 10월 23일

Monobenzone → 2-(4-Benzyloxy-phenoxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/12922

반응식

참여 물질

역할이름HCID투입량
반응물MonobenzoneHCID 7638—
반응물Sodium hydrideHCID 24758—
반응물(R)-tert-Butyl 2-((tosyloxy)methyl)pyrrolidine-1-carboxylateHCID 11760051—
용매DimethylformamideHCID 6228—
생성물2-(4-Benzyloxy-phenoxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 5975302455.6%

반응 단계

To a 15 mL of anhydrous DMF was added NaH (60% dispersion in oil, 338 mg, 8.44 mmol), and the resulting reaction mixture was cooled to 0° C. p-benzyloxy phenol (1.41 g, 7.03 mmol) was added and the reaction mixture was stirred at rt for 45 min. It was then cooled to −5° C., and (R)-Boc-prolinol tosylate (2.5 g, 7.03 mmol) in anhydrous DMF (5 mL) was cooled in a separate ice-bath and added dropwise to the reaction mixture. It was then allowed to warm to rt and stirred at 92° C. for 5 h and at rt overnight. The resulting mixture was poured into 200 mL ice/water and stirred for an hour. The resulting precipitate was filtered, washed with ether, dried over MgSO4, concentrated, recrystallized with ether/hexane to give shiny yellow crystals (1.5 g, 55%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728032B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-188a746988c84b5d953e1fe0403ef6ff
출처 메모uspto-grants-2010_06