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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203Generated: October 26, 2026

Methyl phenoxyacetate → Methyl 4-[3-chloropropanoyl]phenoxyacetate

https://huagongshe.com/reaction/2203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl phenoxyacetateHCID 16365—
Reactant3-Chloropropionyl chlorideHCID 69364—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-[3-chloropropanoyl]phenoxyacetateHCID 18918540—

Reaction Steps

Aluminium chloride (33.35 g) was added portionwise to a stirred cooled (<0° C.) solution of methyl phenoxyacetate (14.46 ml) and 3-chloropropionyl chloride (9.55 ml) in dichloromethane (500 ml). After the addition the ice-bath was removed and the mixture stirred for 1 hour when it was poured into ice-water (500 ml). The organic phase was separated and the aqueous portion extracted two times with dichloromethane. The combined dichloromethane extracts were washed with water, then brine and dried (MgSO4). The residue, after removal of the solvent in vacuo and trituration with ether gave methyl 4-[3-chloropropanoyl]phenoxyacetate, 22.3 g, as a solid: m.p. 89°-90° C.; NMR (d6DMSO) δ 7.95(2H,d), 7.05(2H,d), 4.92(2H,s), 3.91(2H,t), 3.71(3H,s), 3.49(2H,t); m/e 257(M+H)+ ; calculated for C12H13ClO4 : C, 56.1; H, 5.0. found: C, 55.8; H, 5.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728701
Source datasetuspto-grants-1998_03
ORD IDord-4789241e5b8e4d179a6429cc6ce17888
Source noteuspto-grants-1998_03