HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492893Generated: October 30, 2026
2,4,5-Trichlorophenol → 2,4,5-Trichlorophenyl 4-n-Octyloxybenzoate
https://huagongshe.com/reaction/1492893
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,5-Trichlorophenol | HCID 7271 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-(Octyloxy)benzoic acid | HCID 17231 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,4,5-Trichlorophenyl 4-n-Octyloxybenzoate | HCID 616208 | 32% |
Reaction Steps
To a solution of 4-octyloxybenzoic acid (13.8 g) in diethyl ether (552 ml) were added 2,4,5-trichlorophenol (10.87 g) and N,N'-dicyclohexylcarbodiimide (11.37 g). The solution was stirred under a nitrogen atmosphere for 18 hours at room temperature. The precipitate was removed by filtration and the filtrate was concentrated in vacuo. The residue was dissolved in petroleum ether and was allowed to stand on ice-water. The resulting crystals (15.2 g) were filtered and dissolved in warm n-hexane (150 ml). After standing overnight at room temperature, the resulting crystal was removed by filtration. The filtrate was concentrated to an oil which was purified by a column chromatography over silica gel using a mixture of ethyl acetate and n-hexane to give 2,4,5-trichlorophenyl 4-octyloxybenzoate (7.58 g) (MP 53° C., Anal Calcd. for C21H23O3Cl3 : Cl 24.75, Found: Cl 24.05).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05376634 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-ed2def42c30b4090a9998f3005158991 |
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| Source note | uspto-grants-1994_12 |
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