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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486415Generated: October 30, 2026

Sulfuric Acid → 1,1,4,4,5,7-Hexamethyl-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/486415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantM-XyleneHCID 7929—
Reactant3-Chloro-2-methyl-1-propeneHCID 11241—
Product1,1,4,4,5,7-Hexamethyl-1,2,3,4-tetrahydronaphthaleneHCID 13813289—

Reaction Conditions

Temperature20 °C

Reaction Steps

The starting material 1,1,4,4,5,7-hexamethyl-1,2,3,4-tetrahydronaphthalene is prepared by substantially following the procedures of Fehr et al., U.S. Pat. No. 5,162,588. Specifically, in a 1 liter three-neck flask, equipped with a mechanical stirrer and kept under nitrogen, 150.0 g of methallyl chloride are slowly (2 hrs) added to a mixture of meta-xylene (490.9 g) and H2SO4 (30.0 g), while the temperature is maintained at 20° C. After 3 hrs, the H2SO4 is decanted and the organic phase is washed with, in succession, water, an aqueous solution saturated with NaHCO3, and an aqueous solution saturated with NaCl. The excess of meta-xylene is recovered through distillation, and the residue is distilled. A mixture of two isomers, 1-(2-chloro-1,1-dimethylethyl)-2,4-dimethylbenzene and 1-(2-chloro-1,1-dimethylethyl)-3,5-dimethylbenzene, is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292719
Source datasetuspto-grants-1994_03
ORD IDord-45509428ef93463e961b3c9837060dea
Source noteuspto-grants-1994_03