HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(Hexyloxy)phenyl 4-(octyloxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Hexyloxyphenol | HCID 29354 | — |
| Reactant | 4-Octyloxybenzoyl chloride | HCID 2760250 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Hexyloxy)phenyl 4-(octyloxy)benzoate | HCID 15919289 | 50.4% |
Reaction Steps
In tetrahydrofuran were dissolved 1.0 g of p-octyloxybenzoic acid chloride and 800 mg of p-hexyloxyphenol, and 500 mg of triethylamine was added to the solution and reaction was carried out with stirring overnight. The precipitate was removed by filtration, and the filtrate was concentrated, purified by using a silica gel column and recrystallized from ethanol to obtain 800 mg of 4-hexyloxyphenyl 4-octyloxybenzoate. The phase transition temperatures of the so-obtained compounds are as follows. ##STR142##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04925591 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-dc559374cccd4f94ab3db8814e6b6147 |
| Source note | uspto-grants-1990_05 |