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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 4-({[4-(tridecyloxy)phenyl]methyl}amino)benzoate | HCID 13079677 | — |
| Reactant | Water ethanol | HCID 19096565 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-({[4-(Tridecyloxy)phenyl]methyl}amino)benzoic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04350822 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-6b0fc60352e44f62b5401c677a5ad191 |
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| Source note | uspto-grants-1982_09 |
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