Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045818Generated: October 31, 2026

Methyl iodide → HCID 51037313, compound

https://huagongshe.com/reaction/1045818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 58349171HCID 58349171—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 51037313HCID 51037313143.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (17 mg, 0.71 mmol, 1.1 eq) was added to a flame-dried round-bottom flask and anhydrous THF (1.2 mL) was added. The slurry was cooled to 0° C. and compound 10 (164 mg, 0.653 mmol, 1.00 eq) was added as a solution in THF (1.2 mL). After stirring at 0° C. for 30 minutes methyl iodide (44.8 μL, 0.708 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 a tan solid: 1H NMR (400 MHz, CDCl3) δ 8.84 (s, 1H), 8.62 (s, 2H), 8.35 (d, J=2.4 Hz, 1H), 8.30 (d, J=1.9 Hz, 1H), 7.78 (t, J=2.2 Hz, 1H), 3.36 (s, 3H); [M+1]+: 265.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569308B2
Source datasetuspto-grants-2013_10
ORD IDord-83f544a2673a4ef3999d7db84bd6c349
Source noteuspto-grants-2013_10