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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070048Generated: November 2, 2026

Methyl iodide → HCID 59398579, compound

https://huagongshe.com/reaction/2070048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantHCID 17605600HCID 17605600—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59398579HCID 59398579—

Reaction Conditions

Temperature80 °C

Reaction Steps

4-(4-Fluorophenoxy)-3-trifluoromethyl-aniline (1.0 g, 3.7 mmol) was dissolved in THF (5 mL), and di-t-butyl dicarbonate (965 mg, 4.43 mmol) was added thereto. The resulting mixture was stirred at 80° C. for 3 hours. The reaction solution was concentrated. The residue was dissolved in THF (5 mL), and sodium hydride (258 mg, 5.6 mmol) was added thereto. The resulting mixture was stirred at room temperature for 30 minutes, and then iodomethane (348 μL, 5.6 mmol) was added thereto. The mixture was further stirred overnight, and a saturated ammonium chloride aqueous solution was added thereto. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and concentrated under reduced pressure. Then, TFA (2 mL) was added to the residue, followed by stirring for 1 hour at room temperature. The reaction solution was concentrated, and a saturated sodium bicarbonate solution was added thereto. The resulting mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and concentrated under reduced pressure to give a crude product of 4-(4-fluorophenoxy)-3-trifluoromethyl-N-methylaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299252B2
Source datasetuspto-grants-2012_10
ORD IDord-92f84868da914405be96c7b94843a15e
Source noteuspto-grants-2012_10