HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → 4-(1-(Naphthalen-1-ylsulfonyl)piperidin-2-yl)butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 4-(1-(naphthalen-1-ylsulfonyl)piperidin-2-yl)butanoate | HCID 57904267 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | 4-(1-(Naphthalen-1-ylsulfonyl)piperidin-2-yl)butanoic acid | HCID 57904163 | 91.9% |
Reaction Steps
Lithium hydroxide (1.58 g, 65.9 mmol) was added to a solution of methyl 4-(1-(naphthalene-1-ylsulfonyl)piperidine-2-yl)butanoate 3 (4.95 g, 13.18 mmol) in methanol/water (54 ml/36 ml) and the reaction mixture was stirred at room temperature overnight. The completeness of the reaction was checked by means of TLC. When the reaction was complete, the methanol was distilled off under reduced pressure and ethyl acetate was added to the residue. The mixture was acidified with dilute HCl. The aqueous phase was extracted 2× with ethyl acetate and the combined organic phases were dried over Na2SO4 and concentrated under reduced pressure to obtain the desired product 4-(1-(naphthalene-1-ylsulfonyl)piperidine-2-yl)butanoic acid (AC-21) (4.38 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318769B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-cde0d2e1b6a446cbb2e83ad3f06f7d78 |
| Source note | uspto-grants-2012_11 |