関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dibromomethane | HCID 3024 | — |
| 反応物 | Acetyl chloride | HCID 6367 | — |
| 反応物 | Estragole | HCID 8815 | — |
| 反応物 | tert-Butyl methyl ether | HCID 15413 | — |
| 触媒 | Zinc | HCID 23994 | — |
| 触媒 | Cuprous chloride | HCID 62652 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 1-(Cyclopropylmethyl)-4-methoxybenzene | HCID 6422476 | 589.7% |
反応手順
CH2Br2 (220 g) was added to a slurry of zinc powder (340 g) and CuCl (54 g) in diethyl ether (450 ml). The reaction was started by the addition of acetyl chloride (8 g). The reaction mixture was heated to 45° C. and a solution of estragol (192 g) in ether (150 ml) was added during 25 minutes. Additional CH2Br2 (456 g) dissolved in ether (150 ml) was dropped into the grey-red suspension during 45 minutes. Afterwards, the mixture was stirred at 50° C. for 12 hours. The suspension was cooled to room temperature and MTBE (900 ml) was added. The mixture was filtered through celite, and the filtrate was washed with saturated NH4Cl, water, saturated NaHCO3 and brine, dried (MgSO4) and concentrated in vacuo. The residue was distilled (b.p. 90-95° C./0.1 Torr) to yield 97.5 g (46%) of a colorless oil, which was found to have the following characteristics, NMR and MS spectra.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07704942B2 |
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| 出典データセット | uspto-grants-2010_04 |
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| ORD ID | ord-30f4661058b54a008d52b9a20ce7ef92 |
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| 出典メモ | uspto-grants-2010_04 |
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