돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 632562생성일: 2026년 10월 25일

Ethyl Acetate → 1-cyclopentyl N-[1-(tert-butoxycarbonyl)pyrrolidin-3-yl]-L-leucinate

https://huagongshe.com/reaction/632562

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Tert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물L-leucine cyclopentyl ester tosylateHCID 86633653—
용매1,1-DichloroethaneHCID 6365—
생성물1-cyclopentyl N-[1-(tert-butoxycarbonyl)pyrrolidin-3-yl]-L-leucinateHCID 86686416—

반응 단계

To a solution of N-tert-butoxycarbonyl-3-pyrrolidinone (0.382 g, 4.76 mmol) in dichloroethane (20 mL) was added L-leucine cyclopentyl ester tosylate (1.96 g, 5.3 mmol) and sodium triacetoxyborohydride (2.65 g, 12.5 mmol). The mixture was stirred at room temperature for 3 hours, then poured into ethyl acetate (150 mL) and quenched with saturated ammonium chloride solution (50 mL) and washed with saturated sodium hydrogen carbonate solution (3 times 30 mL). The organic extracts were dried (MgSO4), concentrated and purified by flash column chromatography (7:3 ethyl acetate:heptane) to yield the desired product. LC/MS: m/z 369.25 [M+H]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321718B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-6da453aad4f84aac847932ee8559d33c
출처 메모uspto-grants-2016_04