Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920733Generated: October 31, 2026

Aniline → HCID 57733276, compound

https://huagongshe.com/reaction/1920733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantHCID 12249440HCID 12249440—
ProductHCID 57733276HCID 5773327693.1%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 2-(1-ethoxycarbonyl-2-oxo-propyl)-benzoic acid (7.6 g, 30.4 mmol) and aniline (10 ml, 108 mmol) was flushed with argon, sealed in the Emrys process vial and heated at 150° C. for 15 min under microwave irradiation. The volatiles were removed in vacuo and the obtained residue was partitioned between ethyl acetate (100 ml) and 2M HCl (100 ml). The organic layer was washed with brine (2×20 ml), dried (Na2SO4) and evaporated to give 8.7 g of brown oil that solidified. The obtained crude product was of ca. 90% purity according to 1H NMR and can be used in the next step without further purification. Alternatively, the crude product was dissolved in hot ethyl acetate (20 ml), precipitated with heptane (60 ml), allowed to cool, filtered and washed with diethyl ether to give 4.2 g of a pale-brown crystalline solid, yield 45%. LC-MS (m/z) 308.2 (MH+); tR=1.43. 1H NMR (500 MHz, DMSO-d6): 1.34 (t, 3H), 1.97 (s, 3H), 4.41 (q, 2H), 7.38 (d, 2H), 7.51 (t, 1H), 7.56 (t (overlapping m), 3H), 7.62 (d, 1H), 7.8 (t, 1H), 8.22 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173639B2
Source datasetuspto-grants-2012_05
ORD IDord-cee4c566cb6f4c939f45f21a85c02ac6
Source noteuspto-grants-2012_05