HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530173Generated: October 30, 2026
Diethyl Ether → 2,2'-Difluoro-4''-(3-hydroxypropyl)[1,1';4',1'']-terphenyl-4-ol
https://huagongshe.com/reaction/1530173
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol | HCID 54759098 | — |
| Reactant | HCID 67195875 | HCID 67195875 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2'-Difluoro-4''-(3-hydroxypropyl)[1,1';4',1'']-terphenyl-4-ol | HCID 67194886 | — |
Reaction Steps
16.5 g (59 mmol) of sodium metaborate octahydrate and 1.3 g (1.8 mmol) of bis(triphenylphosphine)palladium(II) chloride are initially introduced in 150 ml of water and 50 ml of THF, 12.5 g (38.5 mmol) of 3-(4′-bromo-3′-fluorobiphenyl-4-yl)propan-1-ol are added, and a solution of 12.5 g (0.053 mol) of 3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenol in 50 ml of THF is subsequently added dropwise. The batch is heated under reflux overnight, taken up in MTB ether and washed three times with water. The org. phase is dried over sodium sulfate, the solvent is removed in vacuo, and the crude product is recrystallised from toluene/ethyl acetate (9:1), giving 2,2′-difluoro-4″-(3-hydroxypropyl)[1,1′;4′,1″]-terphenyl-4-ol as colourless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090822B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-1944c11e1a81444584f9066aae90dd51 |
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| Source note | uspto-grants-2015_07 |
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