HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068770Generated: November 4, 2026
Toluene → 5-(3,5-Difluorobenzyl)-2-fluorobenzonitrile
https://huagongshe.com/reaction/2068770
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 3,5-Difluorobenzyl bromide | HCID 518896 | — |
| Reactant | 3-Cyano-4-fluorophenylboronic acid | HCID 2757964 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-(3,5-Difluorobenzyl)-2-fluorobenzonitrile | HCID 44134259 | 129.8% |
Reaction Steps
3-Cyano-4-fluorophenylboronic acid (1.649 g, 10 mmol), powdered potassium phosphate (4.254 g, 20 mmol) and Pd(PPh3)4 (231 mg, 0.2 mmol) were charged in an oven-dried flask under argon atmosphere. The flask was evacuated and back-filled with argon thrice and then toluene (30 mL) and 3,5-difluorobenzyl bromide (1.295 mL, 10 mmol) were added by means of a syringe through a lattice stopper, under good stirring. The reaction mixture was heated to 100° C. in half an hour and maintained at that temperature for 1.5 hours. The black mixture was taken up with diethylether (200 mL), washed with saturated aqueous ammonium chloride (2×20 mL), brine (3×30 mL), dried over sodium sulphate and evaporated to dryness to afford 3.21 g of yellow oil. The crude was purified by flash chromatography on silica gel eluting with n-hexane/ethyl acetate 95:5 to yield 1.89 g (yield 76.4%) of whitish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299057B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-cd506a722532477885b3f6e4c424682c |
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| Source note | uspto-grants-2012_10 |
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