関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-Formylmorpholine | HCID 20417 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 2-Bromo-4-methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene | HCID 59517213 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 4-Methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene-2-carbaldehyde | HCID 59517047 | — |
反応手順
To a solution of 420 mg of 2-bromo-4-methoxy-8,9-dihydro-5,7-dioxa-benzocycloheptene in 10 ml of THF there was added dropwise 0.7 ml of n-butyllithium (2.66 M, hexane solution) at −70° C. under a nitrogen atmosphere. After stirring at −70° C. for 10 minutes, 0.5 ml of N-formylmorpholine was added and the temperature was raised from −70° C. to 0° C. over a period of 30 minutes. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (235 mg) as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07816522B2 |
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| 出典データセット | uspto-grants-2010_10 |
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| ORD ID | ord-e0b48d1b5945417c8e033d5c1089acc4 |
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| 出典メモ | uspto-grants-2010_10 |
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