HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207625Generated: November 1, 2026
1,4-Dioxane → 3-Benzyloxy-4,5-difluoro-phenol
https://huagongshe.com/reaction/2207625
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Di-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphane | HCID 11618717 | — |
| Reactant | 1-Bromo-3-benzyloxy-4,5-difluorobenzene | HCID 57470601 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 3-Benzyloxy-4,5-difluoro-phenol | HCID 89649884 | 60% |
Reaction Steps
To a solution of potassium hydroxide (2246.7 mg, 40.12 mmol) in 1,4-dioxane (5 mL) and Water (5 mL) was added 2-di-tert-butylphosphino-2′,4′,6′-triisopropylbiphenyl (212.63 mg, 0.5015 mmol). The reaction mixture was degassed with nitrogen and then treated with tris(dibenzylideneacetone)dipalladium-[0](183.54 mg, 0.2006 mmol) and 1-benzyloxy-5-bromo-2,3-difluoro-benzene [CAS: 1035155-54-4](3 g, 10.03 mmol) the reaction was then heated at 90° C. for 16 hours. The reaction was diluted with aq. KOH solution (2M, 150 mL) and EtOAc (150 mL). The aqueous was separated, and acidified to pH 1 with aq. HCl (2M). The organics were then extracted into EtOAc (150 mL). The organics were separated, washed with brine (150 mL), dried over MgSO4, filtered and concentrated in vacuo to give crude 3-benzyloxy-4,5-difluoro-phenol ˜60% pure);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376436B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-06037ff7514c44ffb229f87e1ab76e41 |
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| Source note | uspto-grants-2016_06 |
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