HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → alpha-(2-Nitrophenyl)-p-bromocinnamic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | (2-Nitrophenyl)acetic acid | HCID 77337 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | alpha-(2-Nitrophenyl)-p-bromocinnamic acid | HCID 54296204 | 92.5% |
Reaction Steps
A solution of 4-bromobenzaldehyde (27.75 g, 0.150 mol), 2-nitrophenylacetic acid (27.18 g, 0.150 mol) and triethylamine (21.0 ml, 0.150 mol) in 150 ml of acetic anhydride was heated at 40° C. for 38 hours and then poured into 900 ml of water and stirred until the organic layer solidified. The solid was isolated by filtration and dried in vacuo to yield 48.3 g (92%) of the title compound as a tan solid which was sufficiently pure to use directly in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05004739 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-eeb044bd333d44168208e80578af443d |
| Source note | uspto-grants-1991_04 |