関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methane | HCID 297 | — |
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | 3-Chloro-4-methylaniline | HCID 7255 | — |
| 反応物 | HCID 178428198 | HCID 178428198 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | HCID 178428206 | HCID 178428206 | — |
反応手順
A 500 ml., 3-neck, r.b. flask fitted with stirrer, condenser, and thermometer was charged with a mixture of the compound of Example I, C. (21.7 g., 0.1 mole), 3-chloro-4-methylaniline (14.2 g., 0.1 mole) and ethanol (300 ml.). The mixture was heated at reflux, while stirring, overnight. The near solution was concentrated to dryness by rotary evaporator and the residue was collected and dried to yield 35 g. (97.5%), m.p. 352°-364°C (dec). A 10 g. sample was dissolved in methanol (200 ml.), treated with charcoal and filtered while hot. Ether (ca 750 ml.) was added until the filtrate remained turbid and was then chilled. The crystals were collected by filtration and dried to yield 3.4 g. yellow crystals, m.p. 362°-370°C (dec). After two recrystallizations a m.p. 368°-372°C (dec) was obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US03947434 |
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| 出典データセット | uspto-grants-1976_03 |
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| ORD ID | ord-b80aeb6711fb4a458f42da2f0091e636 |
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| 出典メモ | uspto-grants-1976_03 |
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