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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36727Generated: October 28, 2026

Water → 4-(3,5-di-tertiary-butyl-4-hydroxy-N-methylanilino)benzoic acid

https://huagongshe.com/reaction/36727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant4-(3,5-Di-tertiary-butyl-4-hydroxyanilino)benzoic acidHCID 13960406—
SolventMethyl iodideHCID 6328—
Product4-(3,5-di-tertiary-butyl-4-hydroxy-N-methylanilino)benzoic acidHCID 22401583—

Reaction Steps

A solution of 3.4 g (0.010 mole) of 4-(3,5-di-tertiary-butyl-4-hydroxyanilino)benzoic acid (prepared in Example 1) in 35 ml of N,N-dimethylformamide and 3.5 ml of methyl iodide was heated at 95° C. for about 48 hours under nitrogen. The reaction mixture was poured into cold water and the resulting solid was collected and then taken up in chloroform. The chloroform solution was filtered, washed with water, dried with magnesium sulfate and evaporated to give a tan solid. This material was recrystallized first from benzene and then from a mixture of ethanol and water to give 1.5 g of white crystalline 4-(3,5-di-tertiary-butyl-4-hydroxy-N-methylanilino)benzoic acid, m.p. 240°-244° C. Analysis: Calculated for C22H29NO3 : % C, 74.3; % H, 8.2; % N, 3.9. Found: % C, 74.4; % H, 8.3; % N, 3.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05416113
Source datasetuspto-grants-1995_05
ORD IDord-d83919df79ae49428e028e607b0070c2
Source noteuspto-grants-1995_05