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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887460Generated: November 4, 2026

Methyl iodide → HCID 58337588, compound

https://huagongshe.com/reaction/1887460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 58337464HCID 58337464—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 58337588HCID 5833758893%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (24 mg, 1.0 mmol, 1.1 eq) was added to a flame-dried round-bottom flask and anhydrous THF (2.2 mL) was added. The slurry was cooled to 0° C. and compound 34 (255 mg, 0.896 mmol, 1.00 eq) was added as a solution in THF (2.2 mL). After stirring at 0° C. for 30 minutes methyl iodide (61.5 μL, 1.00 mmol, 1.10 eq) was added and the reaction was allowed to warm to room temperature while stirring overnight. The reaction was diluted with EtOAc and washed with water (1×). The aqueous layer was back extracted (1×) with EtOAc and the combined organics were washed with brine, dried (MgSO4), filtered and concentrated in vacuo. Purification by flash chromatography on silica gel afforded 248 mg (93%) of the title compound as an off-white solid: 1H NMR (400 MHz, CDCl3) δ 8.87 (s, 1H), 8.64 (s, 1H), 7.25 (t, J=1.7 Hz, 1H), 7.16 (t, J=1.9 Hz, 1H), 7.07 (t, J=1.9 Hz, 1H), 3.32 (s, 3H); ES-MS [M+1]+: 298.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501757B2
Source datasetuspto-grants-2013_08
ORD IDord-41584301159349b486ab2cb17bdd219d
Source noteuspto-grants-2013_08