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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706000Generated: November 1, 2026

1,2-Dichloro-4-nitrobenzene → Methyl 2-[4-(2-chloro-4-nitrophenoxy)phenoxy]propanoate

https://huagongshe.com/reaction/1706000

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dichloro-4-nitrobenzeneHCID 7443—
ReactantPotassium HydroxideHCID 14797—
ReactantPropanoic acid, 2-(4-hydroxyphenoxy)-, methyl esterHCID 366926—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl 2-[4-(2-chloro-4-nitrophenoxy)phenoxy]propanoateHCID 12883848—

Reaction Steps

6.5 g of pulverised potassium hydroxide and 20 g of methyl 4-hydroxy-α-phenoxypropionate in 250 ml of dry dimethyl sulphoxide are charged at 0° C. into a three-necked flask. With stirring, and at a temperature between 0° and 5° C., 19.5 g of 3,4-dichloro-nitrobenzene are added by small amounts and stirring is continued for 12 hours at room temperature. Thereafter the reaction mixture is poured into ice-water and extracted with ethyl acetate. The extract is dried over sodium sulphate and the solvent distilled off to yield an oily product which is then subjected to high vacuum distillation. The resultant substance, viz. methyl 4-(2'-chloro-4'-nitrophenoxy)-α-phenoxypropionate (yield 27 g), boils at 194° C./0.01 Torr (compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04205978
Source datasetuspto-grants-1980_06
ORD IDord-5bcfcae8317d4c1585cfca2689ab47a7
Source noteuspto-grants-1980_06