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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567738Generated: October 31, 2026

Methyl iodide → HCID 22573170, compound

https://huagongshe.com/reaction/567738

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 numberUS06180632B2
Source datasetuspto-grants-2001_01
ORD IDord-e64f602f7a4848cd95c028599e3f4c7e
Source noteuspto-grants-2001_01