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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1107212생성일: 2026년 10월 25일

Dimethylformamide → Androsta-3,5,16-trien-3-yl Methyl Ether

https://huagongshe.com/reaction/1107212

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물2,2-DimethoxypropaneHCID 6495—
반응물Androsta-4,16-dien-3-oneHCID 92979—
반응물Sodium BicarbonateHCID 516892—
촉매p-Toluenesulfonic acid monohydrateHCID 521998—
용매MethanolHCID 887—
생성물Androsta-3,5,16-trien-3-yl Methyl EtherHCID 1585892144.5%

반응 단계

To a partial solution of androsta-4,16-dien-3-one (1.00 g, 3.70 mmol) in 2.2 dimethoxypropane (5.0 ml, 41 mmol) and 5 ml DMF were added methanol (0.2 ml) and p-toluenesulfonic acid monohydrate (26.4 mg, 0.139 mmol). The mixture was refluxed 5 h, after which it was cooled and sodium bicarbonate (152.5 mg) was added. The suspension was partitioned between 50 ml of ice water and 50 ml of ethyl acetate. The organic layer was washed with two 50 ml portions of water+50 ml of brine, dried over 20 magnesium sulfate, filtered, and concentrated under reduced pressure. The residual oil was taken up in 50 ml of hot hexane and filtered through a 12 mm×30 mm column of silica gel 60 using 150 ml of hot hexane. The combined filtrates were concentrated under reduced pressure and recrystallized from acetone/methanol to give white crystals (468.0 mg, 1.645 mmol, 44%), m.p. 83-92° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06057439
출처 데이터셋uspto-grants-2000_05
ORD IDord-04a5f5a7b71c4ab69388d74e5808a69e
출처 메모uspto-grants-2000_05