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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 567226생성일: 2026년 10월 26일

Benzyl Bromide → 9-[(phenyl)methyl]-5-carbomethoxy-2-methyl-1,2-dihydrocarbazol-4(3H)-one

https://huagongshe.com/reaction/567226

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물5-Carbomethoxy-1,2-dihydro-2-methyl-9H-carbazol-4(3H)-oneHCID 22738715—
용매Hydrochloric AcidHCID 313—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물9-[(phenyl)methyl]-5-carbomethoxy-2-methyl-1,2-dihydrocarbazol-4(3H)-oneHCID 2273883597%

반응 단계

A suspension of 5-carbomethoxy-1,2-dihydro-2-methyl-9H-carbazol-4(3H)-one (2.0 g, 7.77 mM), benzyl bromide (0.94 ml, 7.93 mM), and potassium carbonate (2.15 g, 15.5 mM) in 39 mL DMF was stirred at room temperature for 22 hours. The mixture was diluted with ethyl acetate and 1N HCl. The layers were separated and the aqueous layer extracted with ethyl acetate. The combined ethyl acetate layers were extracted with 1N HCl twice, once with water and once with brine. After drying (NaSO4), evaporation in vacuo afforded 2.61 g (97%) of 9-[(phenyl)methyl]-5-carbomethoxy-2-methyl-1,2-dihydrocarbazol-4(3H)-one. 1H NMR (CDCl3) δ 7.6-7.4 (m, 6H), 7.0 (m, 2H), 5.4 (s, 2H), 4.05 (s, 3H), 3.0 (m, 1H), 2.65-2.45 (m, 3H), 2.3 (dd, J=15 and 9 Hz, 1H), 1.1 (d, J=7 Hz, 3H). MS (ES) m/e 316, 348.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06177440B1
출처 데이터셋uspto-grants-2001_01
ORD IDord-6b3166a4cc87449fb9304fa7d28dd547
출처 메모uspto-grants-2001_01