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HRID 326010作成日:2026年10月25日

2-Chlorotoluene → 2-Chloro-6-nitrotoluene

https://huagongshe.com/reaction/326010

反応式

関与物質

役割名称HCID仕込み量
反応物2-ChlorotolueneHCID 7238—
反応物Benzene, 1-chloro-2-methyl-4-nitro-HCID 83315—
生成物2-Chloro-6-nitrotolueneHCID 674043%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04443630
出典データセットuspto-grants-1984_04
ORD IDord-d37dc916f1ba4f4c875f475a135d219a
出典メモuspto-grants-1984_04