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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703085Generated: October 29, 2026

Acetic Acid → 4-({[4-(Tridecyloxy)phenyl]methyl}amino)benzoic acid

https://huagongshe.com/reaction/1703085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 4-({[4-(tridecyloxy)phenyl]methyl}amino)benzoateHCID 13079677—
ReactantWater ethanolHCID 19096565—
SolventWaterHCID 962—
Product4-({[4-(Tridecyloxy)phenyl]methyl}amino)benzoic acidHCID 13079676—

Reaction Steps

A mixture of 7.0 g. of ethyl p-[(p-tridecyloxybenzyl)amino]benzoate (prepared as described in Example 22), 7.0 g. of potassium hydroxide and 150 ml. of ethanol-water (9:1) is refluxed for 3.5 hours. The solution is acidified while hot, diluted with water, filtered and the solid washed with water to give white crystals, m.p. 110°-113° C. and 145°-150° C. The solid is heated with 200 ml. of glacial acetic acid and the solution chilled and filtered to give crystals, m.p. 110°-112° C. and 155°-160° C. The filtrate is diluted with water to give white crystals (pure by TLC) m.p. 108°-112° C. and 150°-155° C. The first crop of crystals is slurried in 75 ml. of acetone, filtered and the filtrate chilled and filtered. The filtrate is diluted with water to give white crystals (pure by TLC). The two crops pure by TLC are combined, dried in vacuo to give white crystals, m.p. 110°-112° C. and 155°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04350822
Source datasetuspto-grants-1982_09
ORD IDord-6b0fc60352e44f62b5401c677a5ad191
Source noteuspto-grants-1982_09