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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706559Generated: November 1, 2026

Methyl phenylacetate → HCID 12940471, compound

https://huagongshe.com/reaction/1706559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl phenylacetateHCID 7559—
ReactantSuccinic anhydrideHCID 7922—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon DisulfideHCID 6348—
ProductHCID 12940471HCID 12940471—

Reaction Steps

To a mixture of 18 g. of methyl phenylacetate, 26 g. of aluminum chloride and 150 ml. of carbon disulfide, 20 g. of succinic anhydride are added. The reaction mixture is allowed to stand for two hours at 35° C.; then it is added to a liter of ice water and extracted with methylene chloride. The extracts are combined, washed, dried, and evaporated to give methyl p-(3'-carboxy-1'-oxopropyl)-phenylacetate. This derivative is reduced with sodium borohydride and dehydroxylated with palladium charcoal catalyst by the procedures described in Part A of Example 2 to afford methyl p-(3'-carboxypropyl)-phenylacetate. This derivative is refluxed in 50 ml. of thionyl chloride for three hours and then it is evaporated. The residue, containing methyl p-(3'-chlorocarbonylpropyl)-phenylacetate, is taken up in 175 ml. of benzene containing 40 g. of aluminum chloride. The resulting mixture is stirred for two hours at 20° C.; then it is added to a liter of ice and water and extracted with methylene chloride. The extracts are combined, washed with water to neutrality, dried over sodium sulfate, and evaporated to give 7-(methoxycarbonylmethyl)-1-tetralone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207241
Source datasetuspto-grants-1980_06
ORD IDord-99f230c44dcd46c18780b4acbd712675
Source noteuspto-grants-1980_06