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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064227Generated: November 1, 2026

Ethyl Acetate → 7-Fluoro-1H-benzo[d]imidazole-5-carboxylic acid

https://huagongshe.com/reaction/2064227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-7-fluoro-1H-benzo[D]imidazoleHCID 66920500—
CatalystMolybdenum carbonyl (Mo(CO)6)HCID 98885—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product7-Fluoro-1H-benzo[d]imidazole-5-carboxylic acidHCID 6715136863%

Reaction Conditions

Temperature155 °C

Reaction Steps

To a 2.5-5 mL microwave tube, was added 6-bromo-4-fluoro-1H-benzo[d]imidazole (160 mg, 0.744 mmol) suspended in de-gassed 1,4 dioxane (1.5 mL). To this was added trans-di(u-acetato)bis[o-(di-o-tolylphosphino)benzyl]di-palladium (II) (26 mg, 0.043 mmol) and molybdenum hexacarbonyl (100 mg, 0.38 mmol), along with sodium carbonate (237 mg, 2.23 mmol) dissolved in de-gassed water (2 mL). The mixture was stirred for 20 seconds and then heated at 155° C. in the microwave for 10 minutes, keeping the pressure under 16 bar. The vessel was vented before handling and left to stand overnight at room temperature. Water (2 mL) and ethyl acetate (3 mL) were added to the reaction, and then the mixture was filtered through Celite®. The filtrate was partitioned with ethyl acetate and separated. The aqueous fraction was washed with ethyl acetate once more and the combined organic layers were set aside. Another portion of water (5 mL) was added to the aqueous layer and acidified with 0.5 M HCl to pH 3; a brown precipitate was formed. The mixture was allowed to stand in the refrigerator at 4° C. for 1 hour. The mixture was filtered and washed with water to give 4-fluoro-1H-benzo[d]imidazole-6-carboxylic acid as a grey solid, (63% yield). 1H NMR (500 MHz, DMSO-d6) □ ppm 12.99 (br. s., 1H) 8.47 (s, 1H) 8.02 (s, 1H) 7.52 (d, J=11.71 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288405B2
Source datasetuspto-grants-2012_10
ORD IDord-7954a9a352074cfe95ebbd2054d25a68
Source noteuspto-grants-2012_10