Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428222Generated: October 25, 2026

1,1-Dibromoethane → 3-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1-propyne

https://huagongshe.com/reaction/428222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DibromoethaneHCID 11201—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Methoxypropa-1,2-dieneHCID 139403—
Reactant6-Bromo-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthaleneHCID 226685—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product3-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1-propyneHCID 1777386947%

Reaction Conditions

Temperature50 °C

Reaction Steps

20 g (0.82 mol) of magnesium activated with 0.1 ml of dibromoethane are introduced into a four litre reactor under a stream of nitrogen. A solution of 200 g (0.75 mol) of 2-bromo-5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalene is added dropwise so as to maintain the reflux of the THF and the mixture is stirred at 50° C. for two hours. The reaction medium is then cooled to −5° C. and 1.2 g (8.2 mmol) of CuBr are added and a solution of 58 g (0.82 mol) of methoxyallene in 100 ml of THF is introduced dropwise. The mixture is stirred for one hour at −5° C. and is then allowed to return to room temperature and is stirred for two hours. The reaction medium is poured into saturated ammonium chloride solution and extracted with ethyl acetate, and the organic phase is separated out after settling has taken place, dried over magnesium sulphate and evaporated. The oil obtained is distilled at 0.02 mm Hg and the fraction passing at 95-100° C. is collected. 79 g (47%) of the expected product are obtained in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313162B1
Source datasetuspto-grants-2001_11
ORD IDord-6c3aed9c74eb4c98968b6f85f068140e
Source noteuspto-grants-2001_11