関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Oxygen | HCID 977 | — |
| 反応物 | Dimethyl Sulfide | HCID 1068 | — |
| 反応物 | Ozone | HCID 24823 | — |
| 反応物 | Cyclopropanecarboxylic acid, 1-(2-propenyl)-, 1,1-dimethylethyl ester | HCID 546367 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Tert-Butyl 1-(2-oxoethyl)cyclopropanecarboxylate | HCID 58817571 | — |
反応手順
4.0 g (21.9 mmol) of tert-butyl 1-(prop-2-en-1-yl)cyclopropanecarboxylate were dissolved in 70 ml of methanol and 30 ml of dichloromethane. At −78° C., ozone in a stream of O2 was passed through the reaction solution for 45 min using an ozone generator. Once the color of the solution had changed to light blue, the reaction solution was flushed with pure oxygen until the color had disappeared again. 6.5 ml (88.9 mmol) of dimethyl sulfide were then added, and the reaction solution was slowly warmed to RT. The mixture was concentrated on a rotary evaporator and the residue was purified by chromatography on silica gel (mobile phase gradient cyclohexane/ethyl acetate 50:1, 30:1, 20:1, 10:1). This gave 1.87 g (44.1% of theory) of the target compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08642592B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-207b2a0e02ac43db874ec8f41379d8dc |
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| 出典メモ | uspto-grants-2014_02 |
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