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6-ethyl-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene synthesis

2synthesis methods
-

Yield:-

Reaction Conditions:

with iron(III) chloride in ethylbenzene;water;

Steps:

5 Preparation of 1,1,4,4-Tetramethyl-6-Ethyl-1,2,3,4-Tetrahydronaphthalene-7-ol Formate Ester

Specifically, a mixture of 93 g of ethylbenzene and 2 g of anhydrous ferric chloride is cooled to -5° C., and to it is added a solution of 61 g of 2,5-dichloro-2,5-dimethylhexane in 83 g of ethylbenzene during 30 min., maintaining the temperature at -5° C. and agitating continuously. The solution is quenched in water, washed to neutrality and distilled to yield, in addition to the excess of ethylbenzene, 1,1,4,4-tetramethyl-6-ethyl-1,2,3,4-tetrahydronaphthalene.

References:

US5292719,1994,A

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