HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524023Generated: November 4, 2026
Acetonitrile → 6-((2-Bromophenoxy)methyl)picolinonitrile
https://huagongshe.com/reaction/1524023
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Bromophenol | HCID 7244 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 6-Chloromethyl-2-cyanopyridine | HCID 10351875 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-((2-Bromophenoxy)methyl)picolinonitrile | HCID 90313125 | — |
Reaction Steps
To a sealable 4 mL vial, containing 6-(chloromethyl)picolinonitrile (100 mg, 0.66 mmol) and 2-bromophenol (113 mg, 0.66 mmol), were added Cs2CO3 (320 mg, 0.98 mmol) and acetonitrile (1.7 mL). The vial was then heated at 80° Celsius for 15 hours. The reaction was then diluted with ethyl acetate, filtered through a celite plug and concentrated to dryness. The material was used without further purification. 1H NMR (500 MHz, CDCl3) δ 8.02-7.93 (m, 1H), 7.93-7.85 (m, 1H), 7.65-7.59 (dd, J=7.7, 1.1, 1H), 7.58-7.53 (dd, J=7.9, 1.6, 1H), 7.29-7.22 (m, 1H), 6.93-6.90 (dd, J=8.3, 1.3, 1H), 6.90-6.86 (m, 1H), 5.23 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079866B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-a904456bc52d498689fc0cef7eb008ae |
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| Source note | uspto-grants-2015_07 |
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