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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974416Generated: October 29, 2026

Methylsuccinic anhydride → HCID 14234796, compound

https://huagongshe.com/reaction/974416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylsuccinic anhydrideHCID 20051—
Reactant1,1,4,4-TetramethyltetralinHCID 81186—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 14234796HCID 1423479634.2%

Reaction Steps

To a solution of 37.7 g (0.2 mole) of 1,1,4,4-tetramethyl-1,2,3,4-tetrahydro naphthalene and 22.82 g (0.2 mole) of methylsuccinic anhydride in 250 cm3 of anhydrous 1,2-dichloroethane, there are added, by portions, over a period of about 1 hour, 53.3 g (0.4 mole) of anhydrous aluminum chloride in a manner to maintain the temperature lower than or equal to 30° C. After stirring for 3 hours at ambient temperature, the reaction mixture is poured into 200 cm3 of ice water. The organic phase is decanted. The aqueous phase is again extracted twice with 100 cm3 of dichloromethane. The dichloroethane and dichloromethane phases are combined, washed with water, dried on sodium sulfate and concentrated under reduced pressure. The residue is taken up in 300 cm3 of hexane, filtered, successively washed three times with 200 cm3 of toluene and then recrystallized in isopropyl ether. After drying, 20.7 g of 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro- 2-naphthyl)-4-oxo-2-methyl butyric acid in the form of a white solid whose melting point is 165° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05068393
Source datasetuspto-grants-1991_11
ORD IDord-0d5d753b1fbd4a4fa97f3516cb69e37a
Source noteuspto-grants-1991_11