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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 557973생성일: 2026년 10월 25일

Tetrahydrofuran → Benzyl 3-(1,1-dimethylprop-2-en-1-yl)-3-hydroxypyrrolidine-1-carboxylate

https://huagongshe.com/reaction/557973

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물2-Butene, 1-bromo-3-methyl-HCID 70092—
반응물1-N-Cbz-3-pyrrolidinoneHCID 561203—
촉매ZincHCID 23994—
용매Ammonium ChlorideHCID 25517—
생성물Benzyl 3-(1,1-dimethylprop-2-en-1-yl)-3-hydroxypyrrolidine-1-carboxylateHCID 66662637—

반응 단계

To a suspension of benzyl 3-oxopyrrolidine-1-carboxylate (4.50 g, 0.0205 mol) and 4-bromo-2-methyl-2-butene (4.75 mL, 0.0412 mol) in 25.0 mL of saturated ammonium chloride and tetrahydrofuran (4.75 mL, 0.0586 mol) was added zinc (2.70 g, 0.0412 mol) at rt. Soon after stirring was started, gas and heat were evolved. After 45 min., the resulting light grey mixture was filtered through celite. Layers of the filtrate were separated and the aqueous layer of the filtrate was extracted with EtOAc. The organic layers were combined, washed with brine, dried and evaporated in-vacuo. The residue was purified on silica gel, eluting with 0 to 40% EtOAc in hexane, to give the desired product. LCMS (M+Na) 290.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08058288B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-65b6b597bfa9482c91ad92277f821fd0
출처 메모uspto-grants-2011_11