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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899933Generated: November 2, 2026

Methyl iodide → HCID 68792437, compound

https://huagongshe.com/reaction/899933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 2-(3-chloro-4-nitrophenyl)propanoateHCID 13213767—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 68792437HCID 6879243794%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of ethyl 2-(3-chloro-4-nitrophenyl)propanoate (14.1 g) is added dropwise to a suspension of sodium hydride (60% in oil, 2.4 g, 1.1 eq) in DMF (15 ml), cooled down to 0° C. After stirring for 1 hour at this temperature, a solution of methyl iodide (3.72 ml, 1.1 eq) in DMF (40 ml) is added dropwise to the mixture. Stirring is continued for 3 hours at ambient temperature. The reaction medium is cooled down to 0° C. then ethyl acetate, water saturated with sodium hydrogen carbonate are added dropwise, then water. After decantation and extractions, the combined organic phases are washed with salt water, dried over Na2SO4 and concentrated under reduced pressure in order to produce the expected compound in the form of an oil which crystallizes. The crystals are washed with heptane and dried (13.8 g; 94% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07355052B2
Source datasetuspto-grants-2008_04
ORD IDord-c664e9ef71bc4bd68bd83ce1b14bfc5d
Source noteuspto-grants-2008_04