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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 567225생성일: 2026년 10월 26일

Triethylamine → 5-Carbomethoxy-1,2-dihydro-2-methyl-9H-carbazol-4(3H)-one

https://huagongshe.com/reaction/567225

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Tri-o-tolylphosphineHCID 80271—
반응물3-(3-Carbomethoxy-2-bromoanilino)-5-methyl-cyclohex-2-en-1-oneHCID 22740202—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
생성물5-Carbomethoxy-1,2-dihydro-2-methyl-9H-carbazol-4(3H)-oneHCID 2273871575.1%

반응 단계

A suspension of 3-(3-carbomethoxy-2-bromoanilino)-5-methyl-cyclohex-2-en-1-one (9.98 g, 29.5 mM), palladium acetate (0.66 g, 2.95 mM), tri-o-tolylphosphine (1.8 g, 5.9 mM), and triethylamine (5.10 ml, 36.6 mM) in 75 mL acetonitrile was heated at reflux for 3 hours. The solvent was removed in vacuo. The residue was dissolved in methylene chloride, washed with 1 N HCl, then with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated to afford 11 g of crude product. Purification by HPLC on silica gel (elution with gradient methylene chloride/ethyl acetate) afforded 5.7 g (75%) of 5-carbomethoxy-1,2-dihydro-2-methyl-9H-carbazol-4(3H)-one. 1H NMR (CDCl3) δ 9.5 (bs, 1H), 7.4 (d, J=8 Hz, 1H), 7.35 (d, J=8 Hz, 1H), 7.2 (dd, J=8 and 8 Hz, 1H), 4.0 (s, 3H), 2.9 (dd, J=13 and 4 Hz, 1H), 2.55 (m, 2H), 2.4 (m, 1H), 2.25 (dd, J=15 and 9 Hz, 1H), 1.05 (d, J=7 Hz, 3H). MS (ES) m/e 226, 258.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06177440B1
출처 데이터셋uspto-grants-2001_01
ORD IDord-f1c7969d11bb4021a603232b926875a7
출처 메모uspto-grants-2001_01