関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | Phenylboronic Acid | HCID 66827 | — |
| 反応物 | 1-Indanone, 6-bromo- | HCID 139778 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 6-bromo-2-methylene-2,3-dihydro-1H-inden-1-one | HCID 58197166 | 30% |
反応手順
A solution of 6-bromo-2,3-dihydro-1H-inden-1-one (0.3 g, 1.36 mmol), paraformaldehyde (0.4 g, 13.6 mmol), phenylboronic acid (0.2 g, 1.64 mmol) and trifluoroacetic acid (0.1 mL, 0.15 g, 1.36 mmol) in dry toluene (10 mL) was refluxed for 5 hours. When starting material was totally consumed, the crude mixture was cooled to room temperature, neutralized with saturated aqueous Na2CO3, extracted with ethyl acetate, dried and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, petroleum ether-ethyl acetate, 95:5) to give compound 6-bromo-2-methylene-2,3-dihydro-1H-inden-1-one (89 mg, 30%) as a white solid. 1H NMR (CDCl3, 400 MHz): 3.71 (s, 2H), 5.68 (s, 1H), 6.39 (s, 1H), 7.38-7.40 (d, 1H), 7.70-7.72 (d, 1H), 7.99 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09045500B2 |
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| 出典データセット | uspto-grants-2015_06 |
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| ORD ID | ord-4263e9ef95164dd0930c99abca3b5606 |
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| 出典メモ | uspto-grants-2015_06 |
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