HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963005Generated: October 28, 2026
Acetonitrile → 2,6-Difluoro-3-methoxybenzonitrile
https://huagongshe.com/reaction/1963005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2,6-Difluoro-3-methoxybenzamide | HCID 3544383 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,6-Difluoro-3-methoxybenzonitrile | HCID 3791832 | 66% |
Reaction Steps
To an ice cold solution of DMF (0.45 ml) and acetonitrile (10 ml) was added oxalyl chloride (0.41 g, 0.28 ml, 3.20 mmol) dropwise while maintaining the temperature to 0° C. The reaction mixture was stirred at 0° C. for 40 min followed by addition of a solution of 2,6-difluoro-3-methoxybenzamide (0.50 g, 2.70 mmol) in DMF (4.5 ml).The resulting reaction mixture was stirred at 0° C. 40 min and then allowed to come to room temperature. After completion of reaction (10 min, TLC monitoring), triethyl amine (0.57 g, 0.80 ml, 5.67 mmol) was added dropwise. The reaction mass was concentrated in vacuo followed by addition of water (100 ml) and extraction with ethyl acetate (3×100 ml). The combined organics was washed with water, brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified over silica gel (60-120 M, 10% EtOAc-Hexane) to get the desired product (0.30 g, 66%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415383B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-684e7acc92c545c3ab8af53c5a4710b2 |
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| Source note | uspto-grants-2013_04 |
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