関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Ethyl propiolate | HCID 12182 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 4-Methyl-2-nitrobenzaldehyde | HCID 590446 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | Tetrahydrofuran heptane ethylbenzol | HCID 22742125 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Ethyl 4-hydroxy-4-(4-methyl-2-nitrophenyl)-2-butynoate | HCID 18937622 | 98.8% |
反応手順
(a-2) To a solution of ethyl propiolate (1.2 ml, 12.0 mmole) in tetrahydrofuran (20 ml) was added at -65° C. under the argon atmosphere a solution of 2.0M lithium diisopropylamide in a mixed solvent of heptane-tetrahydrofuran-ethylbenzene (6.0 ml, 12.0 mole), and the mixture was stirred for 20 minutes. A solution of 4-methyl-2-nitrobenzaldehyde (1.65 g, 10 mmole) in tetrahydrofuran (10 ml) was added, and the reaction mixture was further stirred at 65° C. for 3 hours. To the reaction mixture was added a saturated aqueous ammonium chloride solution (20 ml) or a solution of acetic acid (13.0 ml, 220 mmole) in tetrahydrofuran (20 ml), followed by water, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with dilute hydrochloric acid, a saturated aqueous sodium hydrogen carbonate solution and a saturated aqueous saline in this sequence, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to give ethyl 4-hydroxy-4-(4-methyl-2-nitrophenyl)-2-butynoate as an oil (2.60 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05840895 |
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| 出典データセット | uspto-grants-1998_11 |
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| ORD ID | ord-38e866aa774a4cdc983f18d941234cc0 |
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| 出典メモ | uspto-grants-1998_11 |
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