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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184817Generated: November 1, 2026

1,2-Dibromoethane → HCID 18399713, compound

https://huagongshe.com/reaction/2184817

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantTris(furan-2-yl)phosphaneHCID 521585—
ReactantTert-butyl 4-iodopiperidine-1-carboxylateHCID 10892302—
ReactantHCID 18399758HCID 18399758—
ReactantDimethylamine tetrahydrofuranHCID 22320367—
CatalystZincHCID 23994—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18399713HCID 18399713—

Reaction Conditions

Temperature65 °C

Reaction Steps

0.16 ml of 1,2-dibromoethane is added at ambient temperature, under argon, to a suspension of 1.35 g of powdered zinc in 10 ml of tetrahydrofuran. The mixture is heated for 5 minutes at 65° C., then brought to ambient temperature, and 0.23 ml of trimethylsilyl is then added. After stirring the mixture for 30 minutes, a solution of 4.5 g of the compound obtained in Step 2 in 8 ml of tetrahydrofuran is slowly added, and then after 45 minutes a solution, prepared ex situ 10 minutes beforehand, of 0.2 g of Pd2(dba)3 and 0.2 g of P(2-furyl)3 in 5 ml of tetrahydrofuran is added by cannulation under argon and, finally, 5.5 g of 1-benzyl-4-bromo-1H-pyrrolo[3,2-c]pyridine in 30 ml of a 1/1 tetrahydrofuran/dimethylamine mixture are added. The reaction mixture is heated at 65° C. for 16 hours and then, after return to ambient temperature, filtered and concentrated in vacuo. Chromatography on silica gel (cyclohexane/ethyl acetate: 50/50) enables the expected product to be isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399616B1
Source datasetuspto-grants-2002_06
ORD IDord-df3bbbc40a7c45daa3411f6697e2bb37
Source noteuspto-grants-2002_06