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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227220Generated: October 31, 2026

Sodium Carbonate → HCID 10735700, compound

https://huagongshe.com/reaction/2227220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTrimethylsilyl triflateHCID 65367—
Reactant2,5,6-Trichloro-1H-benzimidazoleHCID 286009—
ReactantHCID 54135186HCID 54135186—
SolventAcetonitrileHCID 6342—
ProductHCID 10735700HCID 10735700—

Reaction Conditions

Temperature40 °C

Reaction Steps

2,5,6-Trichlorobenzimidazole (221 mg, 1.0 mmol) was suspended in acetonitrile (15 ml) and the mixture was stirred at 40° C. BSA (365 μl, 1.5 mmol) was added, and the reaction mixture stirred for 15 min. A solution of 3 (260 mg, 1.0 mmol) in acetonitrile (5 ml) and TMSOTf (290 μl, 1.5 mmol) was added to the clear solution, and the mixture was allowed to stand at room temperature for 18 hours. The mixture was concentrated under reduced pressure, and the residue was dissolved with dichloromethane (50 ml). The solution was washed with a saturated aqueous solution of sodium bicarbonate (10 ml) and with water (3×10 ml), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was taken up with the minimum amount of dichloromethane and chromatographed on a silica gel column (eluent: gradient of methanol (0-1.6%) in dichloromethane). Fractions having a UV-absorbing spot that also charred under H2SO4 and heating were pooled and concentrated to a foam which was dissolved in ethanol 90 (11 ml). To the stirred solution was added sodium carbonate (216 mg, 2.0 mmol) and the reaction mixture was stirred overnight. The mixture was then evaporated under reduced pressure, dissolved in a 2:1 mixture of ethyl acetate and dichloromethane, and washed with water. The organic layer was dried over sodium sulfate, filtered and evaporated under reduced pressure. Compound 4 crystallized from a 2% methanolic solution of dichloromethane (120 mg, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413938B1
Source datasetuspto-grants-2002_07
ORD IDord-a6814fa19df340d6920b1bc15e43f6e6
Source noteuspto-grants-2002_07