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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519250Generated: October 31, 2026

Sulfuric Acid → HCID 10397005, compound

https://huagongshe.com/reaction/519250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl BromideHCID 6332—
Reactant3a,4,7,7a-Tetrahydro-5-methyl-1,3-isobenzofurandioneHCID 98496—
ReactantMagnesiumHCID 5462224—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10397005HCID 10397005—

Reaction Conditions

Temperature25 °C

Reaction Steps

A 5-L round bottom reaction flask was charged with magnesium metal (Mg) (140 g) and THF (1 L) under nitrogen. Ethyl bromide (EtBr) (630 g) was fed into the reaction mixture dropwise while the temperature was maintained at 25° C. or below using a dry ice bath. After the feeding was completed, the reaction mixture was aged at room temperature for half an hour. Crude 5-methyl-3a,4,7,7a-tetrahydro-isobenzofuran-1,3-dione (1.7 L, ˜56% of the mass of the resulting mixture obtained in EXAMPLE I) was then added dropwise while the temperature was maintained at 25° C. using a dry ice bath. The reaction mixture was consequently further aged at room temperature for another hour. The reaction mixture was poured into sulfuric acid (H2SO4) (10%) containing ice. Toluene was added. The organic and aqueous layers were shaken in a separatory funnel and separated. The aqueous layer was further washed with toluene. The organic layers were combined and washed with sodium carbonate (Na2CO3) solution until basic. The resulting solution was then distilled to afford 3,3-diethyl-5 or 6-methyl-3a,4,7,7a-tetrahydro-3H-isobenzofuran-1-one (457 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115330B2
Source datasetuspto-grants-2015_08
ORD IDord-458e4c53e59d4c699a2c6c9337522270
Source noteuspto-grants-2015_08