HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019755Generated: November 1, 2026
Methanol → 1-Chloro-2-fluoro-4-methoxy-5-nitrobenzene
https://huagongshe.com/reaction/1019755
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Chloro-2,4-difluoro-5-nitrobenzene | HCID 73867 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Chloro-2-fluoro-4-methoxy-5-nitrobenzene | HCID 53403289 | 52% |
Reaction Steps
To a suspension of potassium tert-butoxide (15.07 g, 134.3 mmol) in toluene (100 mL), and the appropriate alcohol, in this case methanol (3.80 g, 118.7 mmol), was added at 0° C. and stirred for 15 minutes. A solution of the appropriate 1-substituted 2,4-difluoro-5-nitrobenzene, in this case 1-chloro-2,4-difluoro-5-nitrobenzene (20.0 g, 103.3 mmol), in toluene (50 mL) was added at 0° C. and stirred for 5 hours at room temperature. Water (1000 mL) was added and the mixture was extracted with EtOAc (3×100 mL). The combined organic extracts were washed with water (150 mL), brine (150 mL), dried (Na2SO4) and concentrated under reduced pressure. The crude residue was purified by column chromatography on neutral silica gel using 5-10% EtOAc in hexane to give the title compound (11.0 g, 52%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716287B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-03b81957356b46d3ac7b10cdf0ba4e2d |
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| Source note | uspto-grants-2014_05 |
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