HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825188Generated: November 2, 2026
Lithium hydroxide, monohydrate → HCID 22143552, compound
https://huagongshe.com/reaction/1825188
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | HCID 22143500 | HCID 22143500 | — |
| Solvent | Tetrahydrofuran dimethanol | HCID 86594347 | — |
| Product | HCID 22143552 | HCID 22143552 | 83% |
Reaction Steps
To a stirred solution of methyl 6-[2-(3-methoxypyrrolidine-1-carbonyl)-thieno[3,2-b]pyridin-7-yloxy]-2-methyl-benzofuran-3-carboxylate 89d (540 mg, 1.16 mmole) in THF/MeOH/MeOH (6 ml, 1:1:1) was added lithium hydroxide monohydrate (54 mg, 1.29 mmole). When the ester disappeared by thin layer chromatography (tic), the organic solvents removed under reduced pressure, and the aqueous residue was neutralized with 2N HCl. The white solid which precipitated was collected by filtration and dried under vacuum to give the desired acid (411 mg, 83%). 1H NMR (DMSO-d6) δ 13.02 (1H, bs), 8.57 (1H,d, J=5.3 Hz), 8.05 (1H, s), 7.94 (1H, d, J=8.5 Hz), 7.68 (1H, s), 7.25 (1H, d, J=8.5 Hz), 6.75 (1H, d, J=5.5 Hz), 4.10–3.85 (3H, m), 3.65–3.45 (2H, m), 3.25 (3H, d, J=9.4 Hz), 2.74 (3H, s), 2.15–1.95 (2H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045528B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-8a5d926f701e4c348d44e42d89fbca11 |
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| Source note | uspto-grants-2006_05 |
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