HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195095Generated: October 31, 2026
Water → 4-(4-Pentenyloxy)biphenyl-4'-carbox-ylic acid 4-(1,1,1-trifluoro-2-octyloxycarbonyl)-phenyl ester
https://huagongshe.com/reaction/1195095
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 1,1,1-Trifluoro-2-octyl 4-hydroxybenzoate | HCID 14549215 | — |
| Reactant | 4-(4-Pentenyloxy) biphenylcarboxylic acid chloride | HCID 54572957 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Pentenyloxy)biphenyl-4'-carbox-ylic acid 4-(1,1,1-trifluoro-2-octyloxycarbonyl)-phenyl ester | HCID 53648251 | — |
Reaction Steps
To 10 ml of methylene chloride were added 0.48 g of 1,1,1-trifluoro-2-octyl 4-hydroxybenzoate, 0.16 g of triethylamine, and a catalytic amount of dimethylaminopyridine, and a solution of 0.57 g of 4-(4-pentenyloxy) biphenylcarboxylic acid chloride in 10 ml of methylene chloride was added slowly thereto under ice-cooling. The reaction mixture was allowed to warm to room temperature, followed by stirring for one day. The reaction mixture was poured into water and extracted with methylene chloride. The methylene chloride phase was washed successively with diluted hydrochloric acid, water, an aqueous 1N sodium carbonate solution, and water and dehydrated over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and the crude product was purified by column chromatography using silica gel to obtain 0.33 g of the titled compound ([α]D20 =+34.3°). The resulting compound exhibited liquid crystal characteristics. The phase transition temperatures of the liquid crystal compound obtained were measured by polarizing microscopic observation using temperature controlled hot stage in which a liquid crystal cell was placed. Phase Transition Temperatures (° C.): ##STR9##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05110498 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-38677198b847430f8bdef7f182994448 |
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| Source note | uspto-grants-1992_05 |
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