HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | methyl (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylate | HCID 10220819 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylic acid | HCID 12050655 | 96.1% |
Reaction Steps
Aqueous lithium hydroxide (1N, 51 ml) was added to a solution of methyl (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylate (8.987 g) [see Preparation 2] in methanol (306 ml) at 0° C. The reaction mixture was stirred at room temperature for 18 hours, after which time the solvent was removed under reduced pressure and the residue partitioned between ethyl acetate and water. The aqueous layer was separated and acidified to pH 2 with 2N aqueous hydrochloric acid, the product was extracted with ethyl acetate, dried over magnesium sulphate and the solvent removed under reduced pressure to afford (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylic acid (8.17 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06372736B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-21c7b15bacb748e2921535e42115c4e7 |
| Source note | uspto-grants-2002_04 |