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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359617Generated: October 30, 2026

Benzyl Chloride → HCID 86743409, compound

https://huagongshe.com/reaction/359617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 45271609HCID 45271609—
ReactantHCID 178418336HCID 178418336—
SolventDiethyl EtherHCID 3283—
ProductHCID 86743409HCID 86743409—

Reaction Steps

6.1 g of (1,2,3,4-tetrahydro-1,1,4,4-tetramethyl-6-naphthyl) ethyl ketone are dissolved in 25 ml of abs. ether and added dropwise at 0° to a benzylmagnesium chloride solution prepared from 0.6 g of magnesium and 4.3 g of benzyl chloride in 30 ml of abs. ether. After stirring at room temperature for 2 hours the reaction mixture is poured into a saturated ammonium chloride solution, extracted with ether, dried over sodium sulphate and evaporated. The thus-obtained oil is dissolved in 100 ml of toluene and, after the addition of 0.5 g of p-toluenesulphonic acid, boiled at reflux overnight. After cooling the mixture is treated with 10% sodium bicarbonate solution, extracted with ether, dried and evaporated. The residue is purified by filtration over a short column (silica gel, elution agent hexane) and recrystallized from methylene chloride/methanol. There are obtained 3 g of 6-(α-ethylstyryl)-1,2,3,5-tetrahydro-1,1,4,4-tetramethylnaphthalene in colourless crystals, melting point 65°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001276
Source datasetuspto-grants-1991_03
ORD IDord-72a1d60278c241a29ddc4adc0ef52926
Source noteuspto-grants-1991_03