HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289379Generated: November 1, 2026
Hydrochloric Acid → 2,3-Difluoro-4'-[12,12-bis(hydroxymethyl)dodecyl]oxybiphenyl
https://huagongshe.com/reaction/1289379
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | 2,3-Difluoro-4'-[12,12-bis(ethoxycarbonyl)dodecyl]oxybiphenyl | HCID 18920838 | — |
| Product | 2,3-Difluoro-4'-[12,12-bis(hydroxymethyl)dodecyl]oxybiphenyl | HCID 18920846 | 71.6% |
Reaction Steps
First, 1.7 g of lithium borohydride and 20 ml of tetrahydrofuran were placed in a 100 ml flask. Then, 60 ml of tetrahydrofuran solution in which 4 g of 2,3-difluoro-4'-[12,12-bis(ethoxycarbonyl)dodecyl]oxybiphenyl was dissolved was added dropwise to the reaction mixture, and the resultant reaction mixture was stirred under reflux for 18 hours. The reaction mixture was poured into cold 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: ethyl acetate/toluene=8/2) and recrystallized from acetone to obtain 2.4 g of 2,3-difluoro-4'-[12,12-bis(hydroxymethyl)dodecyl]oxybiphenyl (Y: 71.6%). The compound thus obtained had a purity of 99.6% by HPLC.
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-272f1f991dfc43899957c3fe45f07873 |
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| Source note | uspto-grants-1998_05 |
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