HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → [1-(4-Acetyl-phenyl)-piperidin-4-YL]-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | [1-(4-Acetyl-phenyl)-piperidin-4-yl]-acetic acid ethyl ester | HCID 57442326 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [1-(4-Acetyl-phenyl)-piperidin-4-YL]-acetic acid | HCID 49759600 | — |
Reaction Steps
To a solution of [1-(4-acetyl-phenyl)-piperidin-4-yl]-acetic acid ethyl ester (20.5 mol) in THF (10 mL) and water (20 mL) is added lithium hydroxide (41 mmol). The resulting mixture is stirred at rt overnight. The organic solvent is evaporated, and the residue is acidified to pH=4-5. The solid is collected by filtration, washed with water and dried at 60° C. in vacuo to give the title compound. 1H NMR (300 MHz, CDCl3) δ 7.86 (2H, d), 6.86 (2H, d), 3.90 (2H, br, d), 2.90 (2H, dt), 2.52 (3H, s), 2.34 (2H, d), 2.04 (1H, m), 1.88 (2H, br, d), 1.39 (2H, ddd); LC-MS (M+1) 262.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851474B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-db3c2aa3340144bf8437a64d460ac7c6 |
| Source note | uspto-grants-2010_12 |