関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dihydrobenzofuran | HCID 10329 | — |
| 反応物 | Methane, dichloromethoxy- | HCID 21004 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2,3-Dihydrobenzofuran-5-carboxaldehyde | HCID 735901 | 60.3% |
反応手順
To a stirred solution of α,α-dichloromethyl methyl ether (2.15 g, 19 mmol, 1.35 eq) in methylene chloride (30 mL) at -40° C. was added successively stannic chloride (1.65 g, 17 mmol, 1.2 eq) and 15 minutes later, a solution of 2,3-dihydrobenzofuran (1.68 g, 14 mmol) in CH2Cl2 (5 mL) maintaining the temperature at or below -35° C. The mixture was warmed to 0° C., stirred 1 hour, then poured into ice-water, and stirred a further 30 minutes. The mixture was diluted with ether, and the phases separated. The organic phase was concentrated in vacuo, and the residue purified by vacuum distillation to yield the title compound (1.25 g, 60%) as a colorless liquid. b.p. 119°-121° C. at 0.3 mm Hg.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05622971 |
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| 出典データセット | uspto-grants-1997_04 |
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| ORD ID | ord-aeae02a3858c4f9190646450ed5f9a61 |
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| 出典メモ | uspto-grants-1997_04 |
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