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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413402생성일: 2026년 10월 24일

N-(tert-butoxycarbonyl)glycine → N-[(1,1-Dimethylethoxy)carbonyl]glycine-4phenylmethoxy-2-butenyl ester

https://huagongshe.com/ko/reaction/413402

반응식

참여 물질

역할이름HCID투입량
반응물N-(tert-butoxycarbonyl)glycineHCID 78288—
반응물cis-4-Benzyloxy-2-buten-1-olHCID 11008492—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물N-[(1,1-Dimethylethoxy)carbonyl]glycine-4phenylmethoxy-2-butenyl esterHCID 69891095—

반응 조건

온도0 °C

반응 단계

N-[(1,1-Dimethylethoxy)carbonyl]glycine (21.9 grams, 0.125 mol), cis-4-benzyloxy-2-buten-1-ol (25 mL, 0.15 mol), and 4-dimethylaminopyridine (1.5 grams, 0.013 mol) are dissolved in methylene chloride and stirred at 0° C. Then N,N-dicyclohexylcarbodiimide (31 grams, 0.15 mol) in 30 mL methylene chloride is added and the reaction is stirred at 0° C. for five minutes. The reaction is then stirred for an additional twelve hours at 25° C. Additional methylene chloride is added and the reaction is washed consecutively with 1 N HCl, sodium bicarbonate and then with brine. The organic extract is dried over magnesium sulfate and the solvent evaporated in vacuo to give an orange oil which is absorbed onto silica gel and applied to a dry silica column. The column is eluted with hexane/EtOAc (9:1) then with hexane/EtOAc (8:2) Product fractions are combined and dried in vacuo to give the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06566381B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-fc51b361b1384d3aa246311f51cb3677
출처 메모uspto-grants-2003_05