HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 2-{[(2E)-3-phenylprop-2-enoyl]amino}benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-(2-Carboxyacetamido)benzoic acid | HCID 439922 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-{[(2E)-3-phenylprop-2-enoyl]amino}benzoic acid | HCID 5717563 | 96.1% |
Reaction Steps
Piperidine (0.42 mL, 4.2 mmol) was added to a suspension of benzaldehyde (0.43 mL, 4.2 mmol) and 2-[(carboxyacetyl)amino]benzoic acid (0.83 g, 3.7 mmol) in toluene (5.0 mL) and treated according to Procedure 2, acidifying with 1 M HCl. (E)-2-[(1-oxo-3-phenyl-2-propenyl)amino]benzoic acid (0.95 g, 96%) was obtained as a pale yellow crystalline solid; mp 188-189° C., lit. [23] 196-197° C.; δH (500 MHz, DMSO-d6) 6.88 (d, J=16.0 Hz, 1H, CH═CHCO), 7.18 (t, J3,4=J4,5=8.0, 1H, H4), 7.41-7.45 (m, 3H, H3′, H4′, H5′), 7.62 (td, J4,5=J5,6=8.0, J3,5=1.5 Hz, 1H, H5), 7.62 (d, J=16.0 Hz, 1H, CH═CHCO), 7.72-7.74 (m, 2H, H2′, H6′), 8.00 (dd, J3,4=8.0, J3,5=1.5 Hz, 1H, H3), 8.59 (d, J5,6=8.0 Hz, 1H, H6), 11.32 (s, 1H, NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765812B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-9332429406f24f12bc8fb1b432693999 |
| Source note | uspto-grants-2014_07 |