Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methyl etherHCID 15413—
Reactant3-Chloro-5-fluoroanilineHCID 2734838—
ReactantSodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
SolventAcetic AcidHCID 176—
Product1-Chloro-3-fluoro-5-nitrobenzeneHCID 2336889118.2%

Reaction Conditions

Temperature55 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334271B2
Source datasetuspto-grants-2016_05
ORD IDord-2b5e73f8363b4225af4525025e69b8b4
Source noteuspto-grants-2016_05