HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522799Generated: October 31, 2026
tert-Butyl methyl ether → 1-Chloro-3-fluoro-5-nitrobenzene
https://huagongshe.com/reaction/522799
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | 3-Chloro-5-fluoroaniline | HCID 2734838 | — |
| Reactant | Sodium;3-oxidodioxaborirane;tetrahydrate | HCID 23693097 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-Chloro-3-fluoro-5-nitrobenzene | HCID 23368891 | 18.2% |
Reaction Steps
Sodium perborate tetrahydrate (7.69 g, 50.0 mmol) was suspended in 30 mL of acetic acid, and this suspension was warmed to 55° C. 3-Chloro-5-fluoroaniline (1.46 g, 10 mmol) was dissolved in 20 mL of acetic acid and added within one hour. The reaction was stirred for 1 hour at 55° C. and then cooled to room temperature. 300 mL of TBME was added, and the reaction mixture was filtered. The organic layer was washed with brine, followed by 20 mL of aqueous Na2S2O3, followed by brine. The organic layer was dried over Na2SO4 and concentrated under reduced pressure to give a residue, which was purified by column chromatography (40 g SiO2; cyclohexane) to yield the title compound as a solid (320 mg, 18%). 1H-NMR (400 MHz; DMSO-d6): 8.20 (s, 1H), 8.18 (d, 1H), 8.07 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334271B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-2b5e73f8363b4225af4525025e69b8b4 |
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| Source note | uspto-grants-2016_05 |
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