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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lithium fluoride | HCID 224478 | — |
| 반응물 | Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine | HCID 353442 | — |
| 반응물 | 1-Benzyl-3,3-difluoropyrrolidine-2,5-dione | HCID 11481520 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (+/-)-cis-2,5-dibenzyl-3a-fluorotetrahydropyrrolo[3,4-c]pyrrole-1,3(2H,3aH)-dione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09290496B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-682af41dad7142ed9d919f31d9f67340 |
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| 출처 메모 | uspto-grants-2016_03 |
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