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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704081Generated: October 30, 2026

Methyl iodide → Methyl 2-(4-chloro-3-methylphenoxy)-2-[p-(p-chlorophenoxy)phenyl]propionate

https://huagongshe.com/reaction/1704081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHexamethylphosphoramideHCID 12679—
ReactantMethyl 2-(p-chlorophenoxy)-2-[p-(p-chlorophenoxy)phenyl]propionateHCID 12531902—
ReactantMethyl (4-chloro-3-methylphenoxy)[p-(p-chlorophenoxy)phenyl]acetateHCID 12531906—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(4-chloro-3-methylphenoxy)-2-[p-(p-chlorophenoxy)phenyl]propionateHCID 20392566—

Reaction Steps

A solution of 0.015 mole of lithium N,N-diisopropylamide (prepared as in example 55) in tetrahydrofuran is chilled to -65° C to -75° C. To the solution is added methyl (4-chloro-3-methylphenoxy)[p-(p-chlorophenoxy)phenyl]acetate in tetrahydrofuran. To the mixture is added 5 ml of hex amethylphosphoramide and while chilling to -65° C to -75° C, 4.26 g of methyl iodide is added. After 1 hr., the mixture is allowed to warm to room temperature and stir overnight. The mixture is poured into water and extracted with ether. The ether extracts are washed with 10% hydrochloric acid, water, saturated NaHCo3, saturaed NaCl solution and dried (MgSO4). Evaporation of the solvent under reduced pressure gives the product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125729
Source datasetuspto-grants-1978_11
ORD IDord-27967b1bd6f742859a95b742a87f3d5e
Source noteuspto-grants-1978_11