関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Hydroxy-5-nitrobenzoyl chloride | HCID 12373909 | — |
| 反応物 | HCID 178509299 | HCID 178509299 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | HCID 178522691 | HCID 178522691 | — |
反応手順
The 5-nitrosalicyloyl chloride thus obtained was dissolved in dry toluene (40 ml) and treated with anhydrous 5-aminotetrazole (3.4 g) and the mixture was stirred and heated at reflux for 12 hours. The mixture was then allowed to cool and was treated with petroleum ether (b.p. 40°-60° C.; 40 ml). The resulting solid was filtered off, washed with petroleum ether (b.p. 40°-60° C.) and stirred with hydrochloric acid (2N; 100 ml). The undissolved solid was filtered off, washed with hydrochloric acid (2N) and with water, and was then dried and dissolved in glacial acetic acid (750 ml). The solution was filtered hot and was then concentrated to 150 ml volume and was then cooled and filtered to give 2-hydroxy-5-nitro-N-(tetrazol-5-yl)-benzamide (2.2 g), m.p. 271°-272° C. (with decomposition).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04146631 |
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| 出典データセット | uspto-grants-1979_03 |
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| ORD ID | ord-bc960eef39e3493d84a57cd5ceff3adc |
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| 出典メモ | uspto-grants-1979_03 |
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