HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815948Generated: October 31, 2026
Benzyl Bromide → 4-(Benzyloxy)-2-fluorobenzonitrile
https://huagongshe.com/reaction/1815948
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoro-4-hydroxybenzonitrile | HCID 2734675 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(Benzyloxy)-2-fluorobenzonitrile | HCID 11333628 | — |
Reaction Steps
A mixture of 2-fluoro-4-hydroxybenzonitrile (15.0 g, 109 mmol), potassium carbonate (21.0 g, 152 mmol), and benzyl bromide (19.6 g, 115 mmol) in acetone (150 mL) under nitrogen was heated at 50° C. overnight. The solid was removed by filtration and the filtrate evaporated to a residue that was mixed with ethyl acetate (500 mL). This solution was washed with brine, dried, and evaporated to give an amorphous solid: (24.9 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06881749B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-6dc1315e4eaf4d598b2284bdd80f843f |
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| Source note | uspto-grants-2005_04 |
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