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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1827911생성일: 2026년 10월 27일

N-Methylmorpholine N-oxide monohydrate → 2-Hydroxy-6-methoxy-3,3-dimethyl-2,3-dihydro-1H-benzo[b]pyrano[3,2-h]-acridine-1,7(14H)-dione

https://huagongshe.com/reaction/1827911

반응식

참여 물질

역할이름HCID투입량
반응물N-Methylmorpholine N-oxide monohydrateHCID 2724197—
반응물6-Methoxy-3,3-dimethyl-3,14-dihydro-7H-benzo[b]pyrano[3,2-h]acridin-7-oneHCID 22064514—
반응물Sodium BisulfiteHCID 23665763—
촉매Osmium TetroxideHCID 30318—
용매tert-ButanolHCID 6386—
용매t-Butanol tetrahydrofuran waterHCID 22124471—
생성물2-Hydroxy-6-methoxy-3,3-dimethyl-2,3-dihydro-1H-benzo[b]pyrano[3,2-h]-acridine-1,7(14H)-dioneHCID 22064508—

반응 단계

To a solution of 1.33 mmol of the compound obtained in Step 2 in 30 ml of a 10/3/1 mixture of tert-butanol/tetrahydrofuran/water there are added osmium tetroxide in the form of a 2.5% solution in 0.67 ml of 2-methyl-2-propanol and 1.35 mmol of 4-methylmorpholine-N-oxide monohydrate. After stirring for two days at ambient temperature, NaHSO3 solution is added. After stirring for one hour, the reaction mixture is extracted with dichloromethane. The organic phase is dried, filtered and then evaporated under reduced pressure. Chromatography of the residue over silica gel (dichloromethane/methanol: 98/2) allows the expected product to be isolated.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07056929B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-f0249d5048814c81ab5e407120ad2ce7
출처 메모uspto-grants-2006_06