関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfur Dioxide | HCID 1119 | — |
| 反応物 | Boron trifluoride etherate | HCID 8000 | — |
| 反応物 | Methyl nitrite | HCID 12231 | — |
| 反応物 | 1-Methoxycyclohexene | HCID 70264 | — |
| 生成物 | Sulfur Dioxide | HCID 1119 | — |
| 生成物 | 1,1-Dimethoxy-2-nitrosocyclohexane | HCID 20336490 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04206112 |
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| 出典データセット | uspto-grants-1980_06 |
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| ORD ID | ord-ef98ad8cd3014b6bbe7983f51a7218d3 |
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| 出典メモ | uspto-grants-1980_06 |
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