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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 442391생성일: 2026년 10월 25일

Sulfur Dioxide → Sulfur Dioxide

https://huagongshe.com/reaction/442391

반응식

참여 물질

역할이름HCID투입량
반응물Sulfur DioxideHCID 1119—
반응물Boron trifluoride etherateHCID 8000—
반응물Methyl nitriteHCID 12231—
반응물1-MethoxycyclohexeneHCID 70264—
생성물Sulfur DioxideHCID 1119—
생성물1,1-Dimethoxy-2-nitrosocyclohexaneHCID 20336490—

반응 단계

1,1-Dimethoxy-2-nitrosocyclohexane dimer was prepared as described in Example 1 from 1-methoxycyclohexene (46.8 g., 0.417 mole), methyl nitrite (30.6 g., 0.501 mole) and boron trifluoride-etherate (0.25 ml., 0.28 g., 2.0 × 10-3 mole) in 250 ml. of sulfur dioxide. The crude nitroso dimer, 76.0 g. of a gummy yellow-green solid still containing traces of sulfur dioxide, was obtained by the method described earlier. Without purification, the dimer was subjected to isomerizing conditions in methanol/sodium methoxide solution. Filtration through celite (to remove colloidal solids that had formed) and evaporation afforded 66.0 g. of an off-white slightly moist solid. Recrystallization from 180 ml. of ether at -70° C. gave 26.8 g. (37.2%) of 1,1-dimethoxy-2-oximinocyclohexane as colorless fine needles, m.p. 112°-116° C. An additional 2.9 g. (4.0%) of slightly impure oxime was obtained from the mother liquor as a white powder, m.p. 105°-112° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04045422
출처 데이터셋uspto-grants-1977_08
ORD IDord-4c0d740083164e6c8a559e8a92617511
출처 메모uspto-grants-1977_08