HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzocaine → 4-[(5-Bromo-pyridin-3-ylmethylene)-amino]-benzoic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzocaine | HCID 2337 | — |
| Reactant | 5-Bromo-3-pyridinecarboxaldehyde | HCID 2784734 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[(5-Bromo-pyridin-3-ylmethylene)-amino]-benzoic acid ethyl ester | HCID 67440476 | 100% |
Reaction Steps
A mixture of 4-amino-benzoic acid ethyl ester (8.06 g, 49 mmol), 5-bromo-pyridine-3-carbaldehyde (10 g, 54 mmol) and p-toluenesulfonic acid (190 mg, 1 mmol) in toluene (300 mL) was heated to reflux for 12 h. Then the reaction mixture cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 4-[(5-bromo-pyridin-3-ylmethylene)-amino]-benzoic acid ethyl ester (16.3 g, 100%) as a light yellow solid: LC/MS m/e calcd for C15H13BrN2O2 (M+H)+: 334.19, observed: 334.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08344137B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-ca7c1f4b39fa4524bcf5108c98ff07fc |
| Source note | uspto-grants-2013_01 |