HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488398Generated: October 29, 2026
Lithium hydroxide, monohydrate → HCID 22264352, compound
https://huagongshe.com/reaction/488398
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Reactant | HCID 22264445 | HCID 22264445 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22264352 | HCID 22264352 | 30% |
Reaction Steps
To a solution of 1-((3,4,5-trimethoxyphenoxy)methyl)carbonyl-2-(methoxycarbonyl)methyl-4-(4-fluorobenzyl)piperazine (0.20 g, 0.42 mmol) in a methanol/water solution (20 mL, 3:1) was added lithium hydroxide, monohydrate (0.40 mL, 9.5 mmol). The resultant mixture was stirred at ambient temperature for 30 min. At that time HPLC analysis showed complete conversion had occurred. The mixture was poured into ethyl acetate and washed sequentially with an aqueous acetic acid/water solution (pH<4), water, and brine. The organic layer was separated, dried over MgSO4, filtered and concentrated in vacuo to afford 0.060 g of 1-((3,4,5-trimethoxyphenoxy)methyl)carbonyl-2-(carboxy)methyl-4-(4-fluorobenzyl)piperazine as a white solid; NMR (CDCl3) 7.4 (m, 2), 7.1 (m, 2), 6.2 (m, 2), 5.1 (m, 1), 4.7 (m, 3), 4.0 (m, 2), 3.8 (d, 9), 3.3-3.1 (m, 4), 2.6 (m, 2), 2.4 (m, 2) ppm, MS (ESI) 476.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06972290B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-613454ad27014b1fa2461edd4b5bc29a |
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| Source note | uspto-grants-2005_12 |
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