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- W2000565952 abstract "Nitration of 2,6-dimethyl-(p-toluenesulpho) anilide or 2,6-dimethyl-benzenesulphoanilide in aqueous acetic acid, followed by deacylation, gives 2,6-dimethyl-4-nitroaniline in yields of 80-90%. These and other procedures are discussed. The rate of deacylation of 2,6-dimethyl-4-nitroacetanilide in sodium methoxide solution is in agreement with the considerable steric inhibition of mesomerism to be expected." @default.
- W2000565952 created "2016-06-24" @default.
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- W2000565952 date "2010-09-02" @default.
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- W2000565952 title "Steric effects on mesomerism: XIII. Preparation of 2,6-dimethyl-4-nitroaniline" @default.
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- W2000565952 doi "https://doi.org/10.1002/recl.19540731004" @default.
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