HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644159Generated: October 29, 2026
Ethanol → 2-(1-Tert-butoxycarbonylpiperidin-4-yloxy)-4-(dimethyl-amino)benzoic acid
https://huagongshe.com/reaction/644159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-(dimethylamino)benzoate | HCID 57602452 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(1-Tert-butoxycarbonylpiperidin-4-yloxy)-4-(dimethyl-amino)benzoic acid | HCID 57602436 | 95% |
Reaction Steps
Potassium hydroxide (3.79 g, 67.5 mmol) in water (135 mL) was added to a mixture of methyl 2-(1-tert-butoxycarbonylpiperidin-4-yloxy)-4-(N,N-dimethylamino)-benzoate (5.11 g, 13.5 mmol) and ethanol. The reaction was heated to 70° C. for 14 hours. The ethanol was removed in vacuo. The resulting aqueous mixture was cooled to 5° C., acidified with satd citric acid, filtered with water wash, and vacuum dried to give the desired product as a white solid (4.65 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07700628B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-209cad99f2ba48e49c5dc6eab4a2c67c |
|---|
| Source note | uspto-grants-2010_04 |
|---|