p-Toluenesulfonic acid → 2-Chlorotoluene-4-sulphonic acid

HRID 1706341

反応式

HRID 1706341 の反応式
[C:1]1([CH3:11])[CH:6]=[CH:5][C:4]([S:7]([OH:10])(=[O:9])=[O:8])=[CH:3][CH:2]=1.[Cl:12]Cl>>[Cl:12][C:2]1[CH:3]=[C:4]([S:7]([OH:10])(=[O:8])=[O:9])[CH:5]=[CH:6][C:1]=1[CH3:11]

参加物

3

実験手順

In a typical process for preparing an aqueous solution of an alkali metal salt of 2-chloro-5-amino-4-toluene sulfonic acid, toluene is first reacted with sulfuric acid to produce para-toluene sulfonic acid as the principal product. The sulfonic acid is then reacted with chlorine to produce 2-chloro-para-toluene sulfonic acid as a principal product which is reacted with a mixture of 50 percent nitric acid and 50 percent sulfuric acid to produce 2-chloro-5-nitro-para-toluene sulfonic acid. The nitrated product is then neutralized in an aqueous lime slurry which is subsequently filtered. The aqueous nitrated product is then iron reduced to form an amine and the reaction mixture is neutralized with sodium hydroxide to a pH of about 9.5-10.5 and the resulting solution is subsequently filtered.

出典と根拠

ORDレコード
ord-869112259f644894a1bd350b276934e3
出典データセット
uspto-grants-1980_06
特許番号
US04207254

関連ノート

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