Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 10-Undecen-1-ol | HCID 8185 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-[4-(4-carboxyphenyl)phenyl]benzoic Acid | HCID 3369891 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 20734023 | HCID 20734023 | — |
Reaction Steps
A suspension of [1,1′;4′,1″]terphenyl-4,4″-dicarboxylic acid (6.37 g, 20 mmol) in 100 ml of thionyl chloride was heated at reflux for 12 h then thionyl chloride was evaporated by azeotropic distillation. The crude yellow residue obtained therefrom was mixed with 10-undecen-1-ol (7.49 g, 44 mmol) in dichloromethane (300 ml) and triethylamine (8.9 g, 88 mmol) was added dropwise to the resulting mixture. The reaction mixture was stirred at 6 h at room temperature, then poured into water (300 ml) and extracted with dichloromethane (2×400 ml). The combined organic extracts were washed with saturated NaCl solution (500 ml), dried over magnesium sulphate, filtered and evaporated to dryness to give a brownish residue which was recrystallised from acetone/dichlorometane: 9/1 to afford pure [1,1′;4′,1″]terphenyl-4,4″-dicarboxylic acid diundec-10-enyl ester as white crystalline material. Yield 8.97 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06749771B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-26920a0238a548b9b170a03db984eb32 |
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| Source note | uspto-grants-2004_06 |
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