HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713446Generated: November 2, 2026
Lithium Hydroxide → [4-(4-Methoxy-3-methyl-benzoyl)-piperidin-1-yl]-acetic acid
https://huagongshe.com/reaction/713446
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | [4-(4-Methoxy-3-methyl-benzoyl)-piperidin-1-yl]-acetic acid ethyl ester | HCID 71226501 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [4-(4-Methoxy-3-methyl-benzoyl)-piperidin-1-yl]-acetic acid | HCID 71227025 | 90% |
Reaction Steps
To a stirred solution of [4-(4-methoxy-3-methyl-benzoyl)-piperidin-1-yl]-acetic acid ethyl ester (0.19 g, 0.60 mmol) in 6 mL of THF and 2 mL of MeOH, was added LiOH (0.13 g, 3.0 mmol in 3 mL of water). After 1.5 hours at ambient temperature the solvent was removed in vacuo, then diluted with 20 mL of water (pH 14). The residue was treated with 12 mL of 1N HCl (pH 4), frozen at −78° C. then lyophilized for 24 hours to yield the title product (0.17 g, 0.54 mmol, 90%) with LiCl salt. MS (ESI) m/z 291.8 (M+H+); HPLC (Novapak 150×3.9 mm C-18 column: mobile phase: 35-90% acetonitrile/water with 0.1% TFA, at 2 mL/min over 2 min.) t 1.58 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181266B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-f2238d890d25468798379579b8b9d1a7 |
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| Source note | uspto-grants-2015_11 |
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