Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376838Generated: October 30, 2026

Dimethyl malonate → Dimethyl [2-[(2-methylphenoxy)methyl]phenyl]propanedioate

https://huagongshe.com/reaction/376838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl malonateHCID 7943—
ReactantSodium hydrideHCID 24758—
Reactant1-Iodo-2-[(2-methylphenoxy)methyl]benzeneHCID 19360029—
SolventHydrochloric AcidHCID 313—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductDimethyl [2-[(2-methylphenoxy)methyl]phenyl]propanedioateHCID 5400101079%

Reaction Steps

To a suspension of sodium hydride (60% oil dispersion) (15.4 g) in 90 mL of 1,3-dimethyl-3,4,5,6-tetrahydro-2 [1H]-pyrimidinone (DMPU), cooled in an ice-water bath, was added dropwise a solution of dimethyl malonate (44 mL) in DMPU (150 mL). The mixture was stirred 20 minutes after the addition was completed, and then 1-iodo-2- [(2-methylphenoxy)methyl]benzene (62.5 g) and cuprous iodide (73.3 g) were added. The resulting mixture was stirred at 100° C. for 5 h, then stirred at 25° C. overnight. The mixture was diluted with 1 N, HCl (~150 mL) and extracted with diethyl ether (3×400 mL). The combined organic extracts were dried (MgSO4), filtered and concentrated under reduced pressure to a semi-solid, which was purified by flash chromatography on silica gel (5:2 hexane: ethyl acetate as eluant). The major material was collected and concentrated to a white solid, which was triturated in hexane and collected by filtration to yield 56.9 g (79%) of the title compound of Step C as a white solid, mp 99-103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022870
Source datasetuspto-grants-2000_02
ORD IDord-4d78685d07394f93ae6b21eb4c37dfd6
Source noteuspto-grants-2000_02