HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39228Generated: October 28, 2026
Hydroquinone → 4-Bromo-1-fluoro-2-isopropenyl-benzene
https://huagongshe.com/reaction/39228
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | 2-(5-Bromo-2-fluorophenyl)propan-2-ol | HCID 66665318 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-1-fluoro-2-isopropenyl-benzene | HCID 58562922 | — |
Reaction Steps
To a solution of 2-(5-bromo-2-fluoro-phenyl)-propan-2-ol (119.7 g, 498 mmol) in CH2Cl2 (50 ml) was added hydrochinone (2.74 g, 24.9 mmol) and 250 ml 85% H3PO4. The resulting reaction mixture was stirred for 3.5 h at 50° C. The mixture was poured onto ice-water and extracted with CH2Cl2. The organic phases were washed with 2N aqueous NaOH and water, dried over MgSO4, filtered and concentrated. The crude product was dissolved in hexane and filtered through a plough of silica gel to obtain after concentration at 600 mbar the title compound as a colorless oil: TLC (hexane): Rf=0.52; UPLC RtH5=1.416 min; 1H NMR (360 MHz, CDCl3): δ 7.43 (dd, 1H), 7.37 (m, 1H), 6.94 (dd, 1H), 5.27 (d, 2H), 2.13 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524897B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-f6a1b92b08954993b26207edf4df9056 |
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| Source note | uspto-grants-2013_09 |
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