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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354508Generated: October 31, 2026

Methyl iodide → HCID 57438725, compound

https://huagongshe.com/reaction/2354508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 57438724HCID 57438724—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57438725HCID 57438725—

Reaction Steps

To a solution of benzyl 2-(5-fluoro-2-pyridyloxy)propionate (2.9 g, 10 mmol) and methyl iodide (3.3 mL, 53 mmol) in 40 mL of anhydrous THF at −78° C. was added potassium hexamethyldisilazide (0.5 M in toluene, 32 mL, 16 mmol). The reaction was allowed to warm to room temperature over 3 h and was partitioned between saturated ammonium chloride (150 mL) and EtOAc (150 mL). The organic layer was separated and the aqueous layer extracted with EtOAc (2×50 mL). The combined organic extracts were dried over anhydrous sodium sulfate, filtered, and concentrated to dryness, and the residue was purified by flash column chromatography on silica gel eluted with 0 to 20% EtOAc in hexane to give the title compound. 1H NMR (500 MHz, CD3OD): δ 7.63 (d, 1H), 7.44 (ddd, 1H), 7.27 (m, 3H), 7.18 (m, 2H), 6.74 (dd, 1H), 5.09 (s, 2H) 1.64 (s, 6H). LC-MS: m/e 290 (M+H)+ (3.7 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754188B2
Source datasetuspto-grants-2010_07
ORD IDord-b75a655a5aec4d76a56154e140042aa6
Source noteuspto-grants-2010_07