Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290466Generated: October 26, 2026

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

https://huagongshe.com/reaction/1290466

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-chloroproponyl 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 C12H13 ClO4 : C, 56.1; H, 5.0. found: C, 55.8; H, 5.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750754
Source datasetuspto-grants-1998_05
ORD IDord-5753f9a3cb4747b8a1b7e982a6e4d239
Source noteuspto-grants-1998_05