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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728559Generated: October 31, 2026

4-Aminophenylacetic acid → HCID 14988368, compound

https://huagongshe.com/reaction/728559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminophenylacetic acidHCID 14533—
Reactant3,5-Di-tert-butyl-4-hydroxybenzoyl chlorideHCID 3787187—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 14988368HCID 1498836811.6%

Reaction Steps

A suspension of 9.2g (0.061 mole) of p-aminophenylacetic acid in 150 ml of 1,2-dimethoxyethane was added to a suspension of 8.0g (0.0298 mole) of 3,5-di-t-butyl-4-hydroxybenzoyl chloride in 100 ml of 1,2-dimethoxyethane, and the resulting mixture was stirred at room temperature for 12 hours. The reaction mixture was then filtered. The filtrate was thereafter diluted with water and chilled. The resulting precipitate was collected and recrystallized from a mixture of ethanol and water to give 1.32g of yellow crystalline 4-(3,5-di-t-butyl-4-hydroxybenzamido)phenylacetic acid, m.p. 253°-254° C. Analysis: Calculated for C23H29NO4 : %C, 72.0; %H, 7.6; %N, 3.6; Found: %C, 72.0; %H, 7.7; %N, 3.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05049572
Source datasetuspto-grants-1991_09
ORD IDord-eb3e593b3df1426689f747cb1c887855
Source noteuspto-grants-1991_09