HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761748Generated: October 25, 2026
Hexanoic Acid → (-)-4-Octyloxy-4'-(1-hexanoyloxyethyl)biphenyl
https://huagongshe.com/reaction/1761748
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexanoic Acid | HCID 8892 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | (+)-4-Octyloxy-4'-(1-butanoyloxyethyl)biphenyl | HCID 19857772 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (-)-4-Octyloxy-4'-(1-hexanoyloxyethyl)biphenyl | HCID 14323892 | 76.3% |
Reaction Steps
Seven grammes (21 mmol) of (-)-1-(4-octyloxybiphenyl-4'-yl)ethanol prepared in Example 2, 7.5 g (36 mmol) of N,N'-dicyclohexylcarbodiimide and 1.0 g of 4-dimethylaminopyridine were dissolved in 200 ml of dichloromethane. To the solution, 3.4 g (29 mmol) of caproic acid was added and the mixture was stirred for six hours at room temperatre. The deposit crystals were filtered, 200 ml of water was added to the filtrate, and the organic layer was separated. 6N hydrochloric acid was added to the organic solution, and then the solution was neutralized with the aqueous solution of 2N sodium hydroxide. The neutralized solution was washed with water until the washed water became neutral. The solvent and low-boiling fractions were distilled off from the obtained solution. The residue was recrystallized from ethanol and the desired (-)-4-octyloxy-4'-(1-hexanoyloxyethyl)biphenyl 6.8 g was obtained. m.p. 60.8° C., [α]D -78.4° (c 0.88, C2H5OH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04827052 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-6b0d047b83d8438c8acec340794c0b33 |
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| Source note | uspto-grants-1989_05 |
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