Phenol → Phenyl 4-chloro-3-nitrobenzenesulfonate

HRID 47084

반응식

HRID 47084 반응식
NC(CCS(OC1C=CC=CC=1)(=O)=O)C(NC1C=CC=CC=1)=O.[N+:24]([C:27]1[CH:28]=[C:29]([S:34](Cl)(=[O:36])=[O:35])[CH:30]=[CH:31][C:32]=1[Cl:33])([O-:26])=[O:25].[C:38]1([OH:44])[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1>>[N+:24]([C:27]1[CH:28]=[C:29]([S:34]([O:44][C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)(=[O:35])=[O:36])[CH:30]=[CH:31][C:32]=1[Cl:33])([O-:26])=[O:25]

참가 물질

4

반응물 3

HCID 996PhenolHCID 7323Benzenesulfonyl chloride, 4-chloro-3-nitro-HCID 203851522-Amino-4-phenoxysulfonyl-butyranilide

생성물 1

HCID 266121Phenyl 4-chloro-3-nitrobenzenesulfonate

실험 절차

Thus, for example, 2-amino-4-phenoxysulfonyl-butyranilide can be obtained by reacting 3-nitro-4-chloro-benzene-sulfonic acid-chloride with phenol to yield 2-nitro-4-phenoxysulfonylchloro-benzene, reacting this product with ammonia to give 2-nitro-4-phenoxy-sulfonyl-aniline, acylating this compound with butyryl-chloride to form 2-nitro-4-phenoxysulfonyl-butyranilide, and by subsequently hydrogenating said product catalytically.

출처 및 근거

ORD 기록
ord-42b221de0f3d4aa6a91e834c6f98940c
출처 데이터셋
uspto-grants-1979_11
특허 번호
US04176192

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