Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014705Generated: November 2, 2026

Tetrahydrofuran → HCID 178518663, compound

https://huagongshe.com/reaction/1014705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantHCID 178419331HCID 178419331—
Reactanttert-Butyl 5-bromo-1H-benzo[d]imidazole-2-carboxylateHCID 178450787—
ProductHCID 178518663HCID 17851866354%

Reaction Steps

tert-Butyl 5-bromo-1H-benzo[d]imidazole-2-carboxylate. A solution of 5-bromo-1H-benzimidazole (1.06 g, 5.38 mmol), di-tert-butyl dicarbonate (1.3 g, 5.91 mmol), triethylamine (0.9 mL, 6.45 mmol) and dimethylaminopyridine (few crystals) in anhydrous tetrahydrofuran (15 mL) was allowed to stir at room temperature overnight. The reaction mixture was concentrated under reduced pressure and the crude product was purified by Biotage chromatography (0-55% ethyl acetate in hexanes) to provide the desired product (0.85 g, 54%) as a white solid. MS (ESI) m/z 297.3 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981893B2
Source datasetuspto-grants-2011_07
ORD IDord-5965746d521e48448d808778af3131c2
Source noteuspto-grants-2011_07