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Hydrochloric Acid → 5-(1-Hydroxy-2-methylprop-2-enyl)furan-2-carboxylic acid benzyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 5-Formyl-2-furancarboxylic acid benzyl ester | HCID 60034788 | — |
| 反応物 | HCID 178455850 | HCID 178455850 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-(1-Hydroxy-2-methylprop-2-enyl)furan-2-carboxylic acid benzyl ester | HCID 86673322 | 94.6% |
反応手順
5-Formyl-2-furancarboxylic acid benzyl ester (300 mg, 1.30 mmol) was dissolved in tetrahydrofuran (12 mL), 2-propenylmagnesium bromide (0.5 mol/L tetrahydrofuran solution, 2.6 mL, 1.3 mmol) was added at −78° C., and the mixture was stirred for 15 minutes. 1N Hydrochloric acid was added to the reaction mixture, the mixture was heated to room temperature and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=70/30) to give the title compound (332 mg, 1.23 mmol, 94%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08877805B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-6bb6b5833c3f4160919148895af1c4d5 |
| 出典メモ | uspto-grants-2014_11 |