HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982026Generated: October 25, 2026
Carbon Dioxide → 1-Benzylbenzimidazole-2-carboxylic acid
https://huagongshe.com/reaction/982026
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Benzyl-1H-benzimidazole | HCID 563347 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzylbenzimidazole-2-carboxylic acid | HCID 20068874 | 80% |
Reaction Steps
A solution of 2.08 g (10 mmol) of 1-benzylbenzimidazole in 200 ml of dry tetrahydrofuran was cooled under N2 atmosphere to -78° C. and treated with 8.0 ml (20 mmol) of n-butyllithium. The resulting solution was warmed to 0° C. for 0.5 h, recooled to -78° C., and poured into a mixture of excess dry ice in 200 ml of tetrahydrofuran. After being allowed to warm, the solution was treated with 200 ml of water, washed with ether, neutralized, and washed with ether. The aqueous layer was concentrated in vacuo, after which the residue was triturated with 2% methanol in chloroform and filtered. The filtrate was dried over MgSO4 and concentrated to give 2.01 g (80%) of the desired compound as a white powder. Mass spectrum: (M-OH)+ =235.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04994477 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-750c5365c4094d608c2b9ce6794daa31 |
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| Source note | uspto-grants-1991_02 |
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