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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 928210생성일: 2026년 10월 25일

Lithium fluoride → (+/-)-cis-2,5-dibenzyl-3a-fluorotetrahydropyrrolo[3,4-c]pyrrole-1,3(2H,3aH)-dione

https://huagongshe.com/reaction/928210

반응식

참여 물질

역할이름HCID투입량
반응물Lithium fluorideHCID 224478—
반응물Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
반응물1-Benzyl-3,3-difluoropyrrolidine-2,5-dioneHCID 11481520—
용매AcetonitrileHCID 6342—
생성물(+/-)-cis-2,5-dibenzyl-3a-fluorotetrahydropyrrolo[3,4-c]pyrrole-1,3(2H,3aH)-dioneHCID 131735057—

반응 단계

To a solution of 1-benzyl-3,3-difluoropyrrolidine-2,5-dione (325 mg, 1.44 mmol) in acetonitrile (3.6 mL), LiF (56 mg, 1.50 eq) and a stir bar were added. The reaction mixture was sonicated for 2.5 hr at rt. N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine (0.4 mL, 1.59 mmol, 1.10 eq) and LiF (37 mg, 1.44 mmol, 1 eq) were added and continued to sonicate for 0.5 hr. The reaction mixture was concentrated and the salt was removed by filtration. The crude residue was purified by column chromatography and eluted with 2 to 20% EtOAc/heptane and purified further with 2 to 10% EtOAc/heptane. The desired fractions were faintly ultraviolet active but were visualized with KMNO4 stain. The title compound was isolated as a yellow oil (196 mg, 40% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.10-7.43 (m, 10 H) 4.57-4.75 (m, 2 H) 3.63 (s, 2 H) 3.56-3.65 (m, 1 H) 3.33-3.41 (m, 1 H) 3.13 (d, J=9.29 Hz, 1 H) 2.74 (dd, J=9.35, 7.03 Hz, 1 H) 2.57-2.70 (m, 1 H). m/z (APCI+) for C20H20FN2O2 339.20 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09290496B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-682af41dad7142ed9d919f31d9f67340
출처 메모uspto-grants-2016_03