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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616727Generated: November 1, 2026

Benzaldehyde → 2-{[(2E)-3-phenylprop-2-enoyl]amino}benzoic acid

https://huagongshe.com/reaction/1616727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
ReactantPiperidineHCID 8082—
Reactant2-(2-Carboxyacetamido)benzoic acidHCID 439922—
SolventTolueneHCID 1140—
Product2-{[(2E)-3-phenylprop-2-enoyl]amino}benzoic acidHCID 571756396.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765812B2
Source datasetuspto-grants-2014_07
ORD IDord-9332429406f24f12bc8fb1b432693999
Source noteuspto-grants-2014_07