HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423125Generated: November 4, 2026
Lithium hydroxide, monohydrate → HCID 23627747, compound
https://huagongshe.com/reaction/1423125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | HCID 23627745 | HCID 23627745 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23627747 | HCID 23627747 | 96% |
Reaction Steps
A solution of [(S)-2-Benzyl-4-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazin-1-yl]-acetic acid methyl ester (342 mg, 0.78 mmol) in THF (5 mL) at room temperature was treated with an aqueous solution (1 mL) containing lithium hydroxide monohydrate (36 mg, 0.86 mmol). The reaction mixture was allowed to stir for 2 h and then evaporated to a small volume. The reaction mixture was then dissolved in water (5 mL) and the pH adjusted to ˜7 with 1 N HCl to precipitate a solid. The precipitate was then triturated with water (2×5 mL) and dried under a stream of nitrogen to afford the title compound as a colorless solid (318 mg, 96%). 1H NMR (CDCl3) 7.27-7.18 (m, 5H), 6.67 (d, J=8.6, 1H), 6.55 (br s, OH), 6.31-6.24 (m, 2H), 4.59-4.57 (m, 1H), 3.89-3.77 (m, 2H), 3.74 (s, 3H), 3.51 (br s, 2H), 3.27 (br s, 3H), 3.15-3.02 (m, 3H), 1.79-1.77 (m, 6H), 1.57-1.43 (m, 2H). LC/MS (Method A) 5.34 min, [M+1]+ 425.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08927546B2 |
|---|
| Source dataset | uspto-grants-2015_01 |
|---|
| ORD ID | ord-5729f04d6d474ca29ba14939c365f0ad |
|---|
| Source note | uspto-grants-2015_01 |
|---|