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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028354Generated: November 3, 2026

1,2-Dibromoethane → HCID 67979279, compound

https://huagongshe.com/reaction/1028354

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantTrimethyl borateHCID 8470—
ReactantMagnesiumHCID 5462224—
Reactant3-Bromo-N,N-diphenylanilineHCID 16217851—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67979279HCID 6797927988%

Reaction Steps

First, 0.45 g of magnesium and 5 ml of THF were suspended, and a tiny amount of 1,2-dibromoethane was added to the obtained suspension. A mixed solution of 3.0 g of 3-bromo-N,N-diphenylaniline and 30 mL of THF was dripped to this suspension, and the mixture was stirred while being heated under reflux for 1.5 hours to cause a reaction. After the reaction, the solution which was naturally cooled to room temperature was cooled to −78° C., and 1.95 g of trimethyl borate was added thereto. The mixture was stirred while the temperature was increased to room temperature to cause a reaction. After the reaction, the solution was concentrated, and 4.8 mL of ethylene glycol and 30 mL of toluene were added to the obtained residue. The mixture was stirred while being heated under reflux for 12 hours to cause a reaction. After the reaction, the solution was filtered and the obtained filtrate was concentrated, so that a while solid was obtained (88% yield). The synthesis scheme of Step 1 is shown by (a-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735581B2
Source datasetuspto-grants-2014_05
ORD IDord-9501879bb27d434cac6e65d657ec377d
Source noteuspto-grants-2014_05