化工社化工社 化学情報印刷レポート · 研究参考用
2-Chlorotoluene → 2-Chloro-6-nitrotoluene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Chlorotoluene | HCID 7238 | — |
| 反応物 | Benzene, 1-chloro-2-methyl-4-nitro- | HCID 83315 | — |
| 生成物 | 2-Chloro-6-nitrotoluene | HCID 6740 | 43% |
反応手順
2-Chloro-5-nitrotoluene, which is required as a starting product, is accessible by nitrating o-chlorotoluene (Rec. Trav. Chim. Pays-Bas 32, (1913) 244 et seq.). It can be isolated from the resulting mixture of isomers by distillation in 43% yield (Loc. cit. 286). This distillation gives pure 2-chloro-6-nitrotoluene as first runnings the other isomers can be separated in a known way. Since all isomers, by virtue of their reactive groups, are intermediates which can be put to many uses and for which there is adequate demand, no undesirable by-products are obtained in this reaction. Thus, even if this preliminary stage is included, this invention represents a very favorable procedure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04443630 |
| 出典データセット | uspto-grants-1984_04 |
| ORD ID | ord-d37dc916f1ba4f4c875f475a135d219a |
| 出典メモ | uspto-grants-1984_04 |