HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913802Generated: November 1, 2026
Hydrochloric Acid → 4-[(4E)-3-(4-Carboxybenzyl)-5-(2-{4-[4-(trifluoromethyl)phenoxy]butoxy}phenyl)pent-4-en-1-yl]benzoic acid
https://huagongshe.com/reaction/1913802
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Propanol | HCID 1031 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 4-[(4E)-3-(4-cyanobenzyl)-5-(2-{4-[4-(trifluoromethyl)phenoxy]butoxy}phenyl)pent-4-en-1-yl]benzoate | HCID 59180514 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[(4E)-3-(4-Carboxybenzyl)-5-(2-{4-[4-(trifluoromethyl)phenoxy]butoxy}phenyl)pent-4-en-1-yl]benzoic acid | HCID 59180485 | — |
Reaction Steps
A solution of 450 mg (0.72 mmol) of methyl 4-[(4E)-3-(4-cyanobenzyl)-5-(2-{4-[4-(trifluoromethyl)phenoxy]butoxy}phenyl)pent-4-en-1-yl]benzoate in 15 ml of 1-propanol and 2 ml of water is mixed with 1207 mg (21.5 mmol) of potassium hydroxide and stirred at 110° C. for 12 h. After cooling, the mixture is acidified with 1 M hydrochloric acid, and the crystals which have separated out are filtered off with suction, washed several times with water and dried. 447 mg (0.65 mmol, 90% of theory, purity 92%) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609727B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-a5dfe1f4a375494ab7a3e9e088b94852 |
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| Source note | uspto-grants-2013_12 |
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