関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Benzoyl chloride, 4-(hexyloxy)- | HCID 170235 | — |
| 反応物 | HCID 178466631 | HCID 178466631 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | HCID 178444959 | HCID 178444959 | 62.1% |
反応手順
In 30 ml of methylene chloride were dissolved 2.1 g of 2-[3-[1-(1H-tetrazol-5-yl)ethoxy]phenoxy]aniline and 2.2 g of triethylamine, followed by dropwise addition of a solution of 1.7 g of 4-hexyloxybenzoyl chloride in benzene with ice-cooling and stirring. The mixture was stirred at room temperature overnight and refluxed for 1 hour. To the reaction mixture was added ice-water and after the mixture was acidified with diluted hydrochloric acid, the methylene chloride layer was separated. The methylene chloride solution was dried over magnesium sulfate and concentrated and the oily residue was subjected to silica gel column chromatography using chloroform-methanol (100:1) as the eluent to give 2.2 g of the title compound as a light yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05399703 |
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| 出典データセット | uspto-grants-1995_03 |
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| ORD ID | ord-3e963d16433042aeab9b5a885ea80189 |
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| 出典メモ | uspto-grants-1995_03 |
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