Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353554Generated: October 31, 2026

Methyl iodide → 1-Chloro-5-(1,1-dimethylethyl)-2-methoxy-3-nitrobenzene

https://huagongshe.com/reaction/2353554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-tert-Butyl-2-chloro-6-nitrophenolHCID 26749—
SolventAcetoneHCID 180—
Product1-Chloro-5-(1,1-dimethylethyl)-2-methoxy-3-nitrobenzeneHCID 57418548—

Reaction Conditions

Temperature65 °C

Reaction Steps

4-tert-Butyl-2-chloro-6-nitro-phenol (0.214 g, 0.934 mmol) was dissolved in 3 mL acetone and K2CO3 (0.65 g, 4.7 mmol) and MeI (0.58 mL, 9.3 mmol) were added. The reaction was stirred at 65° C. overnight, after which the solvent was removed under reduced pressure. The residue was taken up in DCM, the organic layer was washed with water, dried over MgSO4 and concentrated to yield 0.15 g of target product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749999B2
Source datasetuspto-grants-2010_07
ORD IDord-9cd02fd2eb5542fb806b57c17becff29
Source noteuspto-grants-2010_07