HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724247Generated: October 26, 2026
Acetonitrile → 2-Chloro-1-(3-fluoro-benzyloxy)-4-nitro-benzene
https://huagongshe.com/reaction/724247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Nitrofungin | HCID 12074 | — |
| Reactant | 3-Fluorobenzyl bromide | HCID 68007 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-1-(3-fluoro-benzyloxy)-4-nitro-benzene | HCID 7059269 | 95.4% |
Reaction Steps
2-chloro-4-nitrophenol (9.02 g, 52 mmol)), 3-fluorobenzyl bromide (9.85 g, 52 mmol) and acetonitrile (90 mL) was combined at room temperature under nitrogen. Potassium carbonate (7.9 g, 57 mmol)) was added and the reaction mixture stirred at 60° C. for 2 hours and then cooled to room temperature. After cooling the reaction mixture was poured into water. The solids were collected by filtration and washed with diethyl ether to afford the desired product (13.98 g, 95% yield). [TLC system=1:1 EtOAc:Hexanes, Rf=0.76]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141576B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-3b9be54a4a434641b2bbbbcad2610482 |
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| Source note | uspto-grants-2006_11 |
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