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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092669Generated: October 31, 2026

Methyl iodide → HCID 53829389, compound

https://huagongshe.com/reaction/2092669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3-(4-Bromophenyl)propan-1-olHCID 10560614—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53829389HCID 5382938994%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(4-Bromo-phenyl)-propan-1-ol (2.60 g, obtained in example 130, step 1) was dissolved in THF (35 mL). The mixture was cooled to 0° C. and sodium hydride (60% in mineral oil, 967 mg) was added in four portions to the cold mixture. Stirring was continued at 0° C. for 1 hour. Then, iodomethane (1.13 mL) was added dropwise over a period of 15 minutes to the reaction mixture. The mixture was warmed to room temperature over a period of 1 hour. The reaction mixture was poured into ice/water and was extracted two times with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and the solvent was evaporated. The residue was purified by flash chromatography (silica gel, gradient of heptane in ethyl acetate) to give the title compound as a light yellow liquid (2.61 g, 94%). MS (EI): 229.0 [M−].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440710B2
Source datasetuspto-grants-2013_05
ORD IDord-aaf7af42a98247998a3f915f854411a6
Source noteuspto-grants-2013_05