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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 714225생성일: 2026년 10월 25일

Nitrogen → 4-(Benzyloxy)-1-(pyrrolidin-1-yl)butan-1-one

https://huagongshe.com/reaction/714225

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물PyrrolidineHCID 31268—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물4-(Benzyloxy)butanoic acidHCID 562201—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4-(Benzyloxy)-1-(pyrrolidin-1-yl)butan-1-oneHCID 49371180—

반응 단계

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 4-benzyloxybutyric acid (246 mg, 1.27 mmol), pyrrolidine (0.13 mL, 1.52 mmol), EDC.HCl (493 mg, 2.53 mmol), HOBt (262 mg, 1.90 mL) and DIPEA (0.65 mL, 3.80 mmol) in CH2Cl2 (10 mL) was heated at rt until completion of the reaction. Water was added, the layers separated and the aq. layer extracted with CH2Cl2 (2×). The combined org. extracts were washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure. The crude residue was purified by FC (hept-EA, 1:0→0:1) to give 4-(benzyloxy)-1-(pyrrolidin-1-yl)butan-1-one as a colorless oil. LC-MS-conditions 08: tR=0.77 min; [M+H]+=247.95.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09187435B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-e41d7a5469574e83ac8fe401c5c1d186
출처 메모uspto-grants-2015_11