HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromobenzaldehyde → 3-[(3-Bromo-benzylidene)-amino]-4-chloro-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | Methyl 3-Amino-4-chlorobenzoate | HCID 593055 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-[(3-Bromo-benzylidene)-amino]-4-chloro-benzoic acid methyl ester | HCID 67441339 | 99.7% |
Reaction Steps
A mixture solution of 3-amino-4-chloro-benzoic acid methyl ester (21 g, 113.2 mmol), 3-bromo-benzaldehyde (21 g, 113.2 mmol) and p-toluenesulfonic acid (431 mg, 2.2 mmol) in toluene (200 mL) was heated to reflux for 12 hours. Then the reaction mixture was cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 3-[(3-bromo-benzylidene)-amino]-4-chloro-benzoic acid methyl ester (39.8 g, quant.) as a pale-white solid: MS calcd. for C18H11BrClNO2 353.62, obsd. (ESI+) [(M+H)+]351.9 & 353.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586747B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-8bbf468325e64e599f6feae120105a27 |
| Source note | uspto-grants-2013_11 |