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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602130생성일: 2026년 10월 27일

Phthalimide → tert-Butyl 2-((1,3-dioxoisoindolin-2-yl)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/602130

반응식

참여 물질

역할이름HCID투입량
반응물PhthalimideHCID 6809—
반응물TriphenylphosphineHCID 11776—
반응물tert-Butyl 2-(hydroxymethyl)morpholine-4-carboxylateHCID 5201202—
반응물Diethylazodicarboxylate tolueneHCID 66777355—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물tert-Butyl 2-((1,3-dioxoisoindolin-2-yl)methyl)morpholine-4-carboxylateHCID 5899266097%

반응 단계

Triphenylphosphine (506 mg, 1.87 mmol) and phthalimide (275 mg, 1.87 mmol) were added to 4-(tert-butoxycarbonyl)morpholin-2-yl methanol (340 mg, 1.56 mmol) in tetrahydrofuran (3 mL). The mixture was stirred at room temperature for 5 min, followed by addition of a 40% diethyl azodicarboxylate/toluene solution (1.06 mL, 2.34 mmol) and stirring at room temperature for 4 hours. Subsequently, ethyl acetate was added and the mixture washed sequentially with tap water and brine. The mixture was then dried over magnesium sulfate and the solvent was evaporated. Purification of the residue by silica gel column chromatography (hexane:ethyl acetate=10:1->3:1) gave 524 mg (97%) of the desired compound as a colorless powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902367B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-68037ced14ef487da4480e0c343604ce
출처 메모uspto-grants-2011_03