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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633265Generated: October 26, 2026

Methanol → Pentanedioic acid, 2,4-dimethyl-, monomethyl ester

https://huagongshe.com/reaction/1633265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-Methylglutaric anhydrideHCID 77828—
Reactantdihydro-3-methyl-2H-pyran-2,6(3H)-dioneHCID 3015571—
ReactantMethyl 5-chloro-4-methyl-5-oxopentanoateHCID 13192898—
ReactantMethyl 4-chloro-3-methyl-4-oxobutanoateHCID 14403282—
ProductPentanedioic acid, 2,4-dimethyl-, monomethyl esterHCID 549975—

Reaction Steps

The starting materials for said compounds 1, 2, 4, 6, 11 and 12 are the 3-carbomethoxy-2-methylpropanoyl chloride, 2-methylglutaric anhydride, 4-carbomethoxy-2-methylbutanoyl chloride, 3-methylglutaric anhydride and the erythro or threo 4-carbomethoxy-4-(2-phenethyl)-2-methylbutanoyl chloride respectively. That of compound 8 and 9 may be prepared as follows: The solution of 6.0 of meso-2,4-dimethylglutaric acid anhydride [J. Am. Chem. Soc. 77, 1862 (1955)] in 4 ml of methanol is refluxed for one hour and evaporated, to yield the erythro 4-carbomethoxy-2,4-dimethylbutanoic acid. It is converted into the acid chloride by refluxing it with 10.9 g of oxalyl chloride in 50 ml of methylene chloride for 2 hours, and evaporating said mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04479963
Source datasetuspto-grants-1984_10
ORD IDord-6c1697f0a648407e8ce97bd6d40d4f9f
Source noteuspto-grants-1984_10