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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461129Generated: October 27, 2026

1,2-Dibromoethane → HCID 178443368, compound

https://huagongshe.com/reaction/1461129

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
Reactant1-Bromo-3,7-dimethyloctaneHCID 137914—
ReactantMagnesiumHCID 5462224—
Reactant6-Chloro-7-methylene-3-methyl-1-octen-3-yl acetateHCID 11160593—
ReactantHCID 178443371HCID 178443371—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178443368HCID 178443368—

Reaction Steps

In a similar manner to that described in Example 1, a tetrahydrofuran solution of 3,7-dimethyloctylmagnesium bromide was prepared from 6.64 g (0.03 mol) of 3,7-dimethyloctyl bromide, 0.73 g of metallic magnesium, 40 ml of tetrahydrofuran and 3 droplets of ethylene bromide and converted into a tetrahydrofuran solution of 3,7-dimethyloctylzinc chloride by the addition of 4.08 g (0.03 mol) of anhydrous zinc chloride. The subsequent step was conducted with this solution, 0.2 g (0.001 mol) of CuBr·(CH3)2S and 4.4 g (0.02 mol) of 6-chloro-7-methylene-3-methyl-1-octen-3-yl acetate in a similar manner to that described in Example 20 to give 4.1 g of the objective compound as a colorless liquid (yield: 61.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05073659
Source datasetuspto-grants-1991_12
ORD IDord-de217d34892e4e7e9c4ee530ba481659
Source noteuspto-grants-1991_12