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HRID 27168作成日:2026年10月25日
2-((4-Chlorophenyl)amino)acetic acid → N-[2-(3,4-dibenzyloxyphenyl)ethyl]-2-(p-chloroanilino)acetamide
https://huagongshe.com/reaction/27168
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-((4-Chlorophenyl)amino)acetic acid | HCID 230717 | — |
| 反応物 | 3,4-Bis(benzyloxy)phenethylamine hydrochloride | HCID 423869 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | N-[2-(3,4-dibenzyloxyphenyl)ethyl]-2-(p-chloroanilino)acetamide | HCID 20460567 | 50.4% |
反応手順
A mixture of 3,4-dibenzyloxyphenethylamine (36.2 g) and p-chloroanilinoacetic acid (20 g) was stirred for 3 hours at 190° C. The reaction mixture was dissolved in benzene. The solution was washed with a diluted potassium carbonate aqueous solution and dried. The solvent was distilled off from the benzene solution and the residue obtained was purified by column chromatography on silica gel to give N-[2-(3,4-dibenzyloxyphenyl)ethyl]-2-(p-chloroanilino)acetamide (27.2 g), mp 121° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04220647 |
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| 出典データセット | uspto-grants-1980_09 |
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| ORD ID | ord-d32a625541c54a508541c94c4e741306 |
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| 出典メモ | uspto-grants-1980_09 |
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