HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591736Generated: October 29, 2026
Lithium Hydroxide → HCID 178525235, compound
https://huagongshe.com/reaction/1591736
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Oxolane--water (1/1) | HCID 21881883 | — |
| Reactant | ethyl 2-(5,7-bis(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)acetate | HCID 178470769 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178525235 | HCID 178525235 | 114.7% |
Reaction Steps
A solution of ethyl 2-(5,7-bis(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)acetate (250 mg, 0.74 mmol) in 4:1 THF/water (4 mL) was treated with lithium hydroxide (21 mg, 0.88 mmol), and the mixture was stirred overnight. Analysis by LC/MS indicated that the reaction was not complete, so additional lithium hydroxide (5 mg, 0.21 mmol) was added, and the mixture was stirred for 6 h. Analysis by LC/MS indicated that the reaction was still not complete, so additional lithium hydroxide (15 mg, 0.63 mmol) was added, and the mixture was stirred overnight. Analysis by LC/MS indicated that the reaction was complete. The THF was stripped in-vacuo at room temperature, and the aqueous was freeze-dried to yield 270 mg of yellow powder. This material was used as-is in the next step. 1H NMR (500 MHz, CD3OD) δ ppm 3.72 (s, 2 H) 7.54 (s, 1 H) 7.96 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07291615B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-7b0592e14627428cb491cfe5307c7968 |
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| Source note | uspto-grants-2007_11 |
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