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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493523Generated: October 30, 2026

N-bromobutanimide → HCID 19940138, compound

https://huagongshe.com/reaction/1493523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,5-Di(thiophen-2-yl)-1H-pyrroleHCID 4175110—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19940138HCID 1994013846.6%

Reaction Steps

To a solution of 2,5-dithienylpyrrole (130 mg, 0.56 mmol) in 2.5 mL of anhydrous tetrahydrofuran cooled to -78° C. was added N-bromosuccinimide (99.68 mg, 0.56 mmol). After addition was complete the cooling bath was removed and the reaction mixture was allowed to stand in a -20° C. freezer for 4 hours, during which the solution became a brown color. The reaction mixture was concentrated under reduced pressure, carbon tetrachloride was added to precipitate the succinimide, and this mixture was filtered. The filter cake was washed with additional chloroform, the combined filtrates were concentrated, and the resulting oil was chromatographed on silica gel (50 g). Elution with hexane-ethyl acetate, 4:1, furnished 81 mg (46%) of 3-bromo-2,5-dithienylpyrrole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021586
Source datasetuspto-grants-1991_06
ORD IDord-a74c78877163428880338a2ee93e1ad8
Source noteuspto-grants-1991_06