HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-[(2-Bromo-pyridin-4-ylmethyl)-amino]benzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 2-{[(2-bromopyridin-4-yl)methyl]amino}benzoate | HCID 58763671 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[(2-Bromo-pyridin-4-ylmethyl)-amino]benzoic Acid | HCID 23118993 | — |
Reaction Steps
10.0 g (31.2 mmol) of 2-[(2-bromo-pyridin-4-ylmethyl)-amino]-benzoic acid methyl ester is dissolved in 290 ml of ethanol and mixed with 31.2 ml of 2 M sodium hydroxide solution. After having been stirred overnight at room temperature, the ethanol is drawn off, and the aqueous phase is shaken out with ethyl acetate. The aqueous phase is acidified with concentrated hydrochloric acid. The precipitate that is formed is suctioned off and dried. 5.93 g (62%) of 2-[(2-bromo-pyridin-4-ylmethyl)-amino]-benzoic acid accumulates in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07148357B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-60204bbea3c14a739be1e6b92f3b692c |
| Source note | uspto-grants-2006_12 |