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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12970생성일: 2026년 10월 24일

Formaldehyde → (3aR,6aR)-1-(4-Bromophenyl)-5-methyloctahydropyrrolo[3,4-b]pyrrole

https://huagongshe.com/ko/reaction/12970

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Trifluoroacetic acidHCID 6422—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물tert-Butyl(3aR,6aR)-1-(4-bromophenyl)hexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylateHCID 59339923—
용매DichloromethaneHCID 6344—
생성물(3aR,6aR)-1-(4-Bromophenyl)-5-methyloctahydropyrrolo[3,4-b]pyrroleHCID 44221503—

반응 단계

To a solution of (3aR,6aR)tert-butyl 1-(4-bromophenyl)hexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate (1.86 g, 5.1 mmol) in CH2Cl2 (50 mL) at 23° C. was added TFA (8 mL) and the mixture was allowed to stir for 2 hrs. The solvents were removed under vacuum and the residue was taken up in MeOH (50 mL) followed by the addition of formaldehyde (37%, 3 mL, 40 mmol) and NaBH3CN (950 mg, 15.1 mmol). The mixture was stirred at 23° C. for 10 hours, concentrated under reduced pressure and the residue was dissolved in CH2Cl2 (100 mL), washed sequentially with water (2×50 mL), brine (1×30 mL), and dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product mixture was purified via chromatography (SiO2, 0-10% MeOH in CH2Cl2) to provide the title compound. 1H NMR (300 MHz, CDCl3): δ=7.28 ppm (m, 2H), 6.44 (m, 2H), 4.05 (m, 1H), 3.45 (m, 1H), 3.19 (m, 1H), 2.94 (m, 1H), 2.67 (m, 1H), 2.52 (m, 3H), 2.30 (s, 3H), 2.16 (m, 1H), 1.95 (m, 1H). MS (ESI, M+1): 280.8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728031B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-af0a87f14a2a4b51b30e4f209a5f0889
출처 메모uspto-grants-2010_06