HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511188Generated: October 29, 2026
Lithium Hydroxide → HCID 58576150, compound
https://huagongshe.com/reaction/511188
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 4-bromobutyrate | HCID 107604 | — |
| Reactant | 1-(5-Trifluoromethyl-pyridin-2-yl)-piperazine | HCID 667618 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58576150 | HCID 58576150 | 116.4% |
Reaction Steps
A mixture of 1-(5-trifluoromethyl-pyridin-2-yl)-piperazine (370 mg; 1.60 mmol), 4-bromo-butyric acid methyl ester (312 g; 1.60 mmol), potassium carbonate (442 mg; 3.30 mmol) and potassium iodide (265 mg; 1.65 mmol) in acetonitrile (6 mL) is heated to 100° C. for 2 hours. The reaction mixture is allowed to attain room temperature, filtered and the filtrate is concentrated under high vacuum. The resulting residue is taken up in tetrahydrofuran (10 mL) and a solution of lithium hydroxide (115 mg; 4.80 mmol) in water (2 mL) is added. The resulting mixture is stirred at room temperature over night and is then diluted with acetonitrile (90 mL). The precipitate formed is then filtered and dried under high vacuum to afford the desired product (602 mg) which is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096524B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-351734454b8640a8b499504c01723fc0 |
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| Source note | uspto-grants-2015_08 |
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