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Nitric Acid → Phenol, 2,4-dichloro-3-methyl-6-nitro-

HRID 259497
ノート
印刷プレビュー

反応式

HRID 259497 の反応式
ClC1C(C)=CC(O)=CC=1.[S:10]([C:14]1[CH:19]=[C:18]([Cl:20])[C:17]([CH3:21])=[CH:16][C:15]=1[OH:22])([OH:13])(=[O:12])=[O:11].S([C:27]1[CH:32]=[C:31]([Cl:33])[C:30]([CH3:34])=[C:29]([Cl:35])[C:28]=1[OH:36])(O)(=O)=O.[N+:37]([O-])([OH:39])=[O:38].S(=O)(=O)(O)O>>[N+:37]([C:27]1[CH:32]=[C:31]([Cl:33])[C:30]([CH3:34])=[C:29]([Cl:35])[C:28]=1[OH:36])([O-:39])=[O:38].[S:10]([C:14]1[CH:19]=[C:18]([Cl:20])[C:17]([CH3:21])=[CH:16][C:15]=1[OH:22])([OH:13])(=[O:11])=[O:12]
参加物実験手順出典と根拠反応ノート

参加物

7

反応物 5

HCID 944Nitric AcidHCID 1118Sulfuric AcidHCID 17324-Chloro-3-methylphenolHCID 3085507Benzenesulfonic acid, 3,5-dichloro-2-hydroxy-4-methyl-HCID 110423235-Chloro-2-hydroxy-4-methylbenzenesulfonic acid

生成物 2

HCID 170222Phenol, 2,4-dichloro-3-methyl-6-nitro-
HCID 11042323
5-Chloro-2-hydroxy-4-methylbenzenesulfonic acid

実験手順

2-NITRO-4,6-DICHLORO-5-METHYLPHENOL IS PREPARED BY THE SULFONATION OF 4-CHLORO-5-METHYLPHENOL TO FORM 2-SULFO-4-CHLORO-5-METHYLPHENOL WHICH IS CHLORINATED TO 2-SULFO-4,6-DICHLORO-5-METHYLPHENOL WHICH IS IN TURN REACTED WITH NITRIC ACID TO FORM THE DESIRED PRODUCT. The sulfonation is carried out with concentrated sulfuric acid at elevated temperatures to form 2-sulfo-4-chloro-5-methylphenol. Thereafter the reaction mixture is diluted with water to a sulfuric acid content of 20-30%. The resulting 2-sulfo-4-chloro-5-methylphenol is chlorinated with chlorine at elevated temperature and normal or elevated pressures to form 2-sulfo-4,6-dichloro-5-methylphenol which is then reacted with nitric acid.

出典と根拠

ORDレコード
ord-8f514fe2b26543cfad44a0bd46bdb41c
出典データセット
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04038328

反応ノート

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