HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39220Generated: October 23, 2026
Lithium Bromide → 2-Difluoromethoxy-6-nitrobenzonitrile
https://huagongshe.com/en/reaction/39220
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | 2-Bromo-1-(difluoromethoxy)-3-nitrobenzene | HCID 58100766 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Difluoromethoxy-6-nitrobenzonitrile | HCID 58100764 | 84.6% |
Reaction Steps
A mixture of 2-bromo-1-difluoromethoxy-3-nitro-benzene (1 g, 3.7 mmol), CuCN (0.40 g, 4.5 mmol) and LiBr (0.32 g, 3.7 mmol) in tetrahydrofuran (10 ml) are heated in a microwave oven at 200° C. for 40 minutes. The reaction mixture is cooled to ambient temperature, diluted with toluene and washed with aqueous sodium bromide (1M) and aqueous sodium hydrogen sulfite (saturated). The organic phase is dried over sodium sulfate and concentrated. The residue is purified by HPLC to give 2-difluoromethoxy-6-nitrobenzonitrile (0.67 g, 84% yield). 1H-NMR (CDCl3, 400 MHz): 8.20 (d, 1H), 7.85 (t, 1H), 7.75 (d, 1H), 6.75 (t, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524896B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-47972b48f6ac4d3da12438dc0306f2c1 |
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| Source note | uspto-grants-2013_09 |
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