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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23348Generated: October 28, 2026

Methyl iodide → HCID 22573170, compound

https://huagongshe.com/reaction/23348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178486825HCID 178486825—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 22573170HCID 2257317045%

Reaction Steps

A mixture of cis/trans-4-(6,7-dimethoxy-quinoxalin-2-yloxy)-cyclohexanol (170 mg, 0.56 mmole) and NaH (60%, 22.4 mg, 0.56 mmole) in anhydrous THF/DMF (10 mL/2 mL) is stirred at 0° C. for 10 min. before addition of methyl iodide (50 μL, 0.56 mmole). After being stirred at ROOM TEMPERATURE for four hours, the reaction is quenched with water (0.5 mL) and concentrated. The aqueous layer is extracted with methylene chloride (2×20 mL) and the combined organic solutions are washed with brine (5 mL). The residue after concentration is chromatographed on silica gel (30% ethyl acetate/hexane) to give 80 mg (45%) of the desired product (m.p. 85-90° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852712B2
Source datasetuspto-grants-2005_02
ORD IDord-4d03e3e24a874d449b93ba19821482c6
Source noteuspto-grants-2005_02