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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863345Generated: October 30, 2026

Iodoethane → Methyl 2-(p-chlorophenoxy)-2-[p-(p-chlorophenoxy)phenyl]butyrate

https://huagongshe.com/reaction/1863345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHexamethylphosphoramideHCID 12679—
ReactantMethyl(p-chlorophenoxy)[p-(p-chlorophenoxy)phenyl]acetateHCID 12531843—
ReactantMethyl 2-(p-chlorophenoxy)-2-[p-(p-chlorophenoxy)phenyl]propionateHCID 12531902—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(p-chlorophenoxy)-2-[p-(p-chlorophenoxy)phenyl]butyrateHCID 20392631—

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 (p-chlorophenoxy)[p-(p-chlorophenoxy)phenyl]acetate in 10 ml of tetrahydrofuran. To the mixture is added 5 ml of hexamethylphosphoramide and while chilling to -65° C. to -75° C., 4.68 g of ethyl iodide is added. After 1 hr., the mixture is allowed to warm to room temperature and stirr overnight. The mixture is poured into water and extracted with ether. The ether extracts are washed with 10% hydrochloric acid, water, saturated NaHCo3, saturated NaCl solution and dried (MgSO4). Evaporation of the solvent gives the product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04168385
Source datasetuspto-grants-1979_09
ORD IDord-17e1205b157a4a7d855937b538b226d9
Source noteuspto-grants-1979_09