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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1947404생성일: 2026년 10월 25일

1,4-Dibromobenzene → tert-Butyl(3aR,6aR)-1-(4-bromophenyl)hexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate

https://huagongshe.com/reaction/1947404

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참여 물질

역할이름HCID투입량
반응물1,4-DibromobenzeneHCID 7804—
반응물Binap, (A+-)-HCID 634876—
반응물SodiumHCID 5360545—
반응물Butan-1-olateHCID 12476378—
반응물tert-butyl (3aR,6aR)-2,3,3a,4,6,6a-hexahydro-1H-pyrrolo[2,3-c]pyrrole-5-carboxylateHCID 37818785—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물tert-Butyl(3aR,6aR)-1-(4-bromophenyl)hexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylateHCID 59339923—

반응 조건

온도140 °C

반응 단계

tert-Butyl(3aR,6aR)-hexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate (1, 1.5 g, 7.0 mmol), 1,4-dibromobenzene (2.8 g, 20.4 mmol), Pd2(dba)3 (275 mg, 0.3 mmol), BINAP (375 mg, 0.6 mmol) and sodium tent-butoxide (1.93 g, 20.0 mmol) were placed in glass microwave tubes and then purged three times with N2 gas, followed by the addition of toluene (45 mL). The mixture was heated to 140° C. for 15 minutes in a microwave reactor. The mixture was then cooled to room temperature, was filtered, and the crude mixture was purified via chromatography (SiO2, 0-25% ethyl acetate:hexanes) to provide the title compound. 1H NMR (300 MHz, CDCl3): δ=7.30 ppm (m, 2H), 7.39 (m, 2H), 4.11 (m, 1H), 3.57 (m, 3H), 3.31 (m, 3H), 2.99 (m, 1H), 2.15 (m, 1H), 1.92 (m, 1H), 1.43 (s, 9H). MS (ESI, M+1): 310.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399468B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-f79191382e324bc48bbdd9d73c68eddc
출처 메모uspto-grants-2013_03