HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289378Generated: October 26, 2026
Hydrochloric Acid → 2,3-Difluoro-4'-[12,12-bis(ethoxycarbonyl)dodecyl]oxybiphenyl
https://huagongshe.com/reaction/1289378
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2,3-Difluoro-4'-(11-bromoundecyl)oxybiphenyl | HCID 18920856 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3-Difluoro-4'-[12,12-bis(ethoxycarbonyl)dodecyl]oxybiphenyl | HCID 18920838 | 84.7% |
Reaction Steps
First, 0.62 g of sodium ethoxide, 1.5 g of diethyl malonate, and 50 ml of dry ethanol were placed in a 100 ml flask whose content was replaced with argon. Then, 20 ml of tetrahydrofuran solution in which 4 g of 2,3-difluoro-4'-(11-bromoundecyl)oxybiphenyl was dissolved was added dropwise to the reaction mixture, and the resultant reaction mixture was stirred under reflux for 8 hours. The reaction mixture was poured into diluted hydrochloric acid, and an organic layer was extracted with ether. The ether layer was washed with water and dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away. The residue was purified by silica gel column chromatography (eluent: toluene) to obtain 4 g of 2,3-difluoro-4'-[12,12-bis(ethoxycarbonyl)dodecyl]oxybiphenyl (Y: 84.7%). The compound thus obtained had a purity of 99.8% by GC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05750213 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-737b20e0ab864dca948446b5066447cd |
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| Source note | uspto-grants-1998_05 |
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