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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029844Generated: November 2, 2026

4-Amino-2,6-di-tert-butylphenol → 2-[N-(3,5-Di-t-butyl-4-hydroxyphenyl)carbamoyl]-transcyclohexanecarboxylic Acid

https://huagongshe.com/reaction/1029844

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2,6-di-tert-butylphenolHCID 314220—
Reactant(-)-trans-1,2-Cyclohexanedicarboxylic AnhydrideHCID 12261141—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-[N-(3,5-Di-t-butyl-4-hydroxyphenyl)carbamoyl]-transcyclohexanecarboxylic AcidHCID 1504487553.3%

Reaction Steps

A solution containing 4.00 g (0.022 mole) of 4-amino-2,6-di-t-butylphenol in 50 ml of 1,2-dimethoxye-thane was added dropwise over a period of ten minutes to a solution of 3.35 g (0.022 mole) of trans-1,2-cyclohexanedi-carboxylic anhydride in 50 ml of 1,2-dimethoxyethane. The reaction mixture was stirred at room temperature for about seventy-two hours. The solvent was removed under vacuum and the residual solid was triturated with a mixture of diethyl ether and hexane. The resulting solid was recrys-tallized from a mixture of ethyl acetate and hexane to give 4.4 g of white solid 2-[N (3,5-di-t-butyl-4-hydroxyphenyl) carbamoyl]-trans-cyclohexanecarboxylic acid, m.p. 247°-252° C. Analysis: Calculated for C: HNO. %C, 70.4; %H, 8.9; %N, 3.7; Found: %C, 70.4; %H, 8.9; %N, 3.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05103037
Source datasetuspto-grants-1992_04
ORD IDord-b1a6eac8213b48edb7ee35c751654e63
Source noteuspto-grants-1992_04