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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 729443생성일: 2026년 10월 27일

Phthalimide → 2-(1-Benzyl-3-methoxymethylpyrrolidin-3-ylmethyl)isoindole-1,3-dione

https://huagongshe.com/reaction/729443

반응식

참여 물질

역할이름HCID투입량
반응물PhthalimideHCID 6809—
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(1-Benzyl-3-methoxymethylpyrrolidin-3-yl)methanolHCID 21979083—
용매TetrahydrofuranHCID 8028—
생성물2-(1-Benzyl-3-methoxymethylpyrrolidin-3-ylmethyl)isoindole-1,3-dioneHCID 5783263721.9%

반응 단계

A solution of (1-benzyl-3-methoxymethylpyrrolidin-3-yl)methanol (Example A19, 1.71 g, 7.27 mmol), triphenylphosphine (2.16 g, 8.22 mmol), phthalimide (1.14 g, 7.73 mmol), and anhydrous tetrahydrofuran is cooled to 0° C. and treated with diethyl azodicarboxylate (1.62 g, 9.31 mmol). The resulting mixture is stirred at room temperature for 18 hours and concentrated under vacuum. The residue is purified by flash column chromatography (1:5 ethyl acetate/hexanes) to afford the title compound, (0.58 g) as a solid. 1H NMR (200 MHz, CDCl3): δ 7.91-7.80 (m, 2H), 7.78-7.66 (m, 2H), 7.39-7.11 (m, 5H), 3.95-3.72 (m, 2H), 3.65-3.40 (m, 2H), 3.31 (s, 2H), 3.27 (s, 3H), 2.72-2.34 (m, 4H), 2.02-1.82 (m, 1H), 1.76-1.56 (m, 1H). MS ES: m/z 365 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582627B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-c70012a30c4d46d0b299918c255e5ae2
출처 메모uspto-grants-2009_09