HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419937Generated: October 30, 2026
Water → 1-[1-(2-Hydroxyethyl)-1H-benzimidazol-7-yl]ethanone
https://huagongshe.com/reaction/419937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-(2-Hydroxyethyl)-1H-benzimidazole-7-carbonitrile | HCID 11446781 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Product | 1-[1-(2-Hydroxyethyl)-1H-benzimidazol-7-yl]ethanone | HCID 58298500 | 80% |
Reaction Steps
A solution of 1-(2-hydroxyethyl)-1H-benzimidazole-7-carbonitrile (0.29 g, 1.5 mmol) in dry THF (6.2 ml) is cooled to −78° C. and MeLi (5.8 mL, 9.3 mmol) is added slowly. After the addition the reaction mixture is allowed to warm up to ambient temperature and kept such for 30 min. The temperature is brought down to −78° C. again and water (4 ml) was added slowly. After warming up the reaction mixture is acidified to pH 4 and heated at 50° C. for 30 min. Solvents are removed under reduced pressure and the residue is partitioned between ethyl acetate and aq. NaHCO3. The organic extract is further washed with water and brine, dried over Na2SO4 and concentrated. Purification is performed on flash silica column using ethyl acetate-methanol as the eluent to give the desired product (0.25 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093402B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-e00ec58703fc4c8fa52f786dfcfa1c38 |
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| Source note | uspto-grants-2012_01 |
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