돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 627생성일: 2026년 10월 24일

2-Bromo-4-nitrotoluene → N-(2-methyl-5-nitrophenyl)oxetan-3-amine

https://huagongshe.com/ko/reaction/627

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-4-nitrotolueneHCID 82189—
반응물Oxetan-3-amine hydrochlorideHCID 23062080—
시약Cesium carbonateHCID 10796—
촉매Palladium (II) acetateHCID 4144353—
촉매(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine;Ferrocene, 1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-, (2R)-HCID 144543273—
생성물N-(2-methyl-5-nitrophenyl)oxetan-3-amineHCID 8049407928.82%

반응 조건

온도90 °C

반응 단계

2-bromo-1-methyl-4-nitrobenzene (864 mg, 4mmol), oxetan-3-amine hydrochloride (438 mg, 4 mmol), CS2CO3 (3910 mg, 12.00 mmol), palladium(II) acetate (44.9 mg, 0.20 mmol), (R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t- butylphosphine (224 mg, 0.40 mmol) in 1,4-doxane was degased, inflated with Ar and heated at 90 oC for 5h. LCMS showed some product peak. Silica gel 2g was added to the mixture, evaporated all solvents in GeneVac. The sample was dry loaded for purification by ISCO (Hexane/EtOAc=100/10-100/50) N-(2-methyl-5-nitrophenyl)oxetan-3-amine (240 mg, 28.8 %) 1H NMR (400 MHz, CD2Cl2) d: 7.47 (dd, 1H), 7.14 (d, 1H), 6.98 (s, 1H), 4.99 (t, 2H), 4.63 (m, 1H), 4.46 (t, 2H), 4.20(m, 1H), 2.18 (s, 3H). LCMS: 209 [M+H]+.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-85488250153944e595f74578eeba1555
출처 메모750 AstraZeneca ELN dataset