HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728519Generated: October 31, 2026
Triethylamine → 4-[[4'-(Octyloxy)-4-biphenylyl]carbonyloxy]benzoic acid 1-(trifluoromethyl)heptyl ester
https://huagongshe.com/reaction/1728519
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(4-Octyloxyphenyl)benzoyl chloride | HCID 11078473 | — |
| Reactant | 1,1,1-Trifluoro-2-octyl 4-hydroxybenzoate | HCID 14549215 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[[4'-(Octyloxy)-4-biphenylyl]carbonyloxy]benzoic acid 1-(trifluoromethyl)heptyl ester | HCID 14766965 | — |
Reaction Steps
To a mixture of the 1,1,1-trifluoro-2-octyl 4-hydroxybenzoate prepared above (0.53 g) and triethylamine (0.18 g) in methylene chloride (10 ml) was slowly added under ice cooling a solution of 4-n-octyloxybiphenyl-4'-carboxylic acid chloride (0.73 g) in methylene chloride (10 ml). After the mixture was left to stand until it reached room temperature, it was stirred overnight. The mixture was poured in water and extracted with methylene chloride. The extracted layer was washed with dilute aqueous hydrochloric acid solution, water, 1N aqueous sodium carbonate solution and water, in this order, and dehydrated over anhydrous magnesium sulfate. After the solution was distilled under reduced pressure to remove the solvent, the residue was purified by silica-gel column chromatography to obtain the titled compound (0.4 g, [α]D20 =+32.2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05328641 |
|---|
| Source dataset | uspto-grants-1994_07 |
|---|
| ORD ID | ord-2fdd760dab554777912ece06e6a7aac2 |
|---|
| Source note | uspto-grants-1994_07 |
|---|