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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantLithium ChlorideHCID 433294—
Reactant[4-(4-Methoxy-3-methyl-benzoyl)-piperidin-1-yl]-acetic acid ethyl esterHCID 71226501—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product[4-(4-Methoxy-3-methyl-benzoyl)-piperidin-1-yl]-acetic acidHCID 7122702590%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181266B2
Source datasetuspto-grants-2015_11
ORD IDord-f2238d890d25468798379579b8b9d1a7
Source noteuspto-grants-2015_11