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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505883Generated: November 2, 2026

Methyl iodide → Methyl 2-(4-(methylthio)phenyl)acetate

https://huagongshe.com/reaction/505883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Methylthio)phenylacetic acidHCID 4983912—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(4-(methylthio)phenyl)acetateHCID 1206766297%

Reaction Steps

1.82 g (10 mmol) of the 4-methylthiophenylacetic acid were dissolved in 30 mL of DMF and 1.34 g (16 mmol) of NaHCO3 are then added; the agitation mixture is stirred for 15 min approx. Next, 1.9 mL of ICH3 are added while keeping agitation at room temperature for 24 h. Once this time elapsed the mixture is poured on water/ice. As no precipitation occurs ether is added and extracted. The organic phase is washed with water and after drying on sodium sulfate anhydride, the organic phase is concentrated in a rotary evaporator getting 1.92 g (9.7 mmol, 97% yield) of colorless oil which spectroscopic data confirm the expected structure. This product will be used in the next step of the synthesis process without purification as it provides a single stain in TLC (eluting dichloromethane/methanol 9/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781594B2
Source datasetuspto-grants-2010_08
ORD IDord-0b25af229efc46c7a0c16a34b36e92b5
Source noteuspto-grants-2010_08