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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995884Generated: October 30, 2026

Ethyl Bromide → 1-(1,2,3,4-Tetrahydro-4,4-dimethyl-1-naphthalenyl)-1-propanone

https://huagongshe.com/reaction/1995884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantMagnesiumHCID 5462224—
ReactantHCID 54561769HCID 54561769—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
Product1-(1,2,3,4-Tetrahydro-4,4-dimethyl-1-naphthalenyl)-1-propanoneHCID 16644564%

Reaction Steps

223 g (1 mol) of 1,1-dimethyl-tetralin-4-carboxylic acid chloride and 11 g of copper (I) iodide are placed in a 1-liter flask provided with a thermometer, stirrer, dropping funnel and reflux condenser and there is allowed to drop in from the dropping funnel at -10° C. to -5° C. a Grignard solution freshly prepared from 27 g (1.1 mol) of magnesium shavings and 122 (1.12 mol) of ethyl bromide in 500 ml of absolute ether. In so doing, the mixture must be diluted with a small amount of ether. The mixture is stirred for a further 5 hours while cooling and then the cooling source is removed. After the mixture has reached room temperature, it is poured into cold, saturated ammonium chloride solution, extracted with ether, washed neutral with water, dried over sodium sulphate and evaporated. Fractional distillation gives 138 g of 1,1-dimethyl-4-propionyl-tetralin of boiling point 75° C./0.05 mmHg; nD20 =1.5263; yield 64%. Ventilation can further improve the olfactory quality. Odour: see (3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04406828
Source datasetuspto-grants-1983_09
ORD IDord-e6c061b8fe3f445b8123e6d53e9b9c56
Source noteuspto-grants-1983_09