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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177521Generated: October 27, 2026

Methyl iodide → HCID 59438472, compound

https://huagongshe.com/reaction/2177521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-(2-Methoxy-4-trifluoromethyl-phenyl)-4,4-dimethyl-4,5-dihydro-oxazoleHCID 59438535—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59438472HCID 59438472—

Reaction Steps

To a solution of 5.465 g (20 mmol) 2-(2-methoxy-4-trifluoromethyl-phenyl)-4,4-dimethyl-4,5-dihydro-oxazole in 60 ml dry THF were added at <−60° C. 11.0 ml (22 mmol) lithium diisopropylamide solution 2M in THF/heptanes/ethylbenzene and the mixture stirred for 1.5 h at <−60° C. To the resulting dark brown solution were added 2.5 ml (40 mmol) iodomethane drop wise over 10 min (exothermal, Ti<−48° C.). The resulting light brown solution was stirred at <−50° C. for 2.5 h then quenched with sat. aq. NH4Cl solution and extracted three times with tert-butyl methyl ether. The combined organic phases were washed 3× with brine, dried over Na2SO4, filtered and evaporated: 7.002 g yellow solid: which was purified by flash-chromatography on silica gel with heptane and 5 to 10% AcOEt over 25 min and heptane/AcOEt 90:10 for 20 min to provide the title compound as a light yellow oil. MS (m/e): 288.12 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067911B2
Source datasetuspto-grants-2015_06
ORD IDord-c4300f2d387c4b54a844fede9063d4e1
Source noteuspto-grants-2015_06