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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12378생성일: 2026년 10월 24일

Phthalimide → (S)-(+)-N-(2,3-Epoxypropyl)phthalimide

https://huagongshe.com/ko/reaction/12378

반응식

참여 물질

역할이름HCID투입량
반응물PhthalimideHCID 6809—
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(-)-GlycidolHCID 6973630—
용매TetrahydrofuranHCID 8028—
생성물(S)-(+)-N-(2,3-Epoxypropyl)phthalimideHCID 71941273.9%

반응 조건

온도0 °C

반응 단계

To a cold solution of (S)-1-oxiranylmethanol (5 g, 67.5 mmol) and phthalimide (9.9 g, 67.3 mmol) in tetrahydrofuran (200 mL) in ice bath was added triphenylphosphine (17.9 g, 68.2 mmol) and diethyl azodicarboxylate (12.3 g, 70.6 mmol). The mixture was stirred at 0° C. for 2 h and at ambient temperature for 48 h. The mixture was concentrated under vacuum, and the oily residue was purified by flash silica column chromatography, yielding the desired product (10.1 g) as pale yellow solid: Rf=0.51 in 1:1 EtOAc/hexane. 1H—NMR (CDCl3, 300 MHz): δ (ppm) 7.76-7.64 (m, 2H), 7.63-7.60 (m, 2H), 3.9-3.8 (dd, 1H), 3.70-3.65 (dd, 1H), 3.15 (m, 1H), 2.70-2.67 (dd, 1H), 2.58-2.55 (dd, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728006B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0fb31da23a524499978fccaaf3c41b28
출처 메모uspto-grants-2010_06