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Ethyl Acetate → methyl 5-formyl-(R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]-pentanecarboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Ozone | HCID 24823 | — |
| 反応物 | methyl (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]-6-heptenoate | HCID 86743990 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 生成物 | methyl 5-formyl-(R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]-pentanecarboxylate | HCID 86743989 | — |
反応手順
A solution of 2.56 g of methyl (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]-6-heptenoate in 40 ml of ethyl acetate was treated with ozone at -75° C. After completion of the reaction 0.1 g of Pd-on-carbon was added thereto and the mixture was hydrogenated at room temperature. After the hydrogen uptake was finished the catalyst was filtered off and washed with ethyl acetate and the filtrate and washings were evaporated in vacuo. There was obtained methyl 5-formyl-(R)-3[(tetrahydro-2H- pyran-2-yl)oxy]pentanecarboxylate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05246960 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-1961c38b3bfe41e9850737dd3646a122 |
| 出典メモ | uspto-grants-1993_09 |