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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062676Generated: November 2, 2026

Ethyl 3-(m-nitrophenyl)-3-oxopropionate → HCID 10447091, compound

https://huagongshe.com/reaction/1062676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(m-nitrophenyl)-3-oxopropionateHCID 104078—
ReactantThioureaHCID 2723790—
ReactantHydroxy tosyloxy iodobenzeneHCID 21918218—
SolventAcetonitrileHCID 6342—
ProductHCID 10447091HCID 1044709171%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of ethyl 3-(3-nitrophenyl)-3-oxopropionate (3.45 g, 14.5 mmol) in 100 mL of acetonitrile was added hydroxy(tosyloxy)iodobenzene (6.3 g, 16.0 mmol). The resulting suspension was stirred at 65° C. for 1 h at which time the reaction was a homogeneous solution. Thiourea (1.22 g, 16.0 mmol) was added and stirring was continued at 65° C. for 2 h. The mixture was cooled and concentrated, and the residue was taken up in ethyl acetate, washed with saturated aq Na2CO3 and brine, dried (MgSO4) and concentrated. The residue was triturated with ethyl ether to afford 3.0 g (71%) of the title compound as a yellow solid. 1H NMR (DMSO-d6) δ: 8.47 (t, 1H, J=1.9 Hz); 8.24 (m, 1H) ; 8.21 (m, 1H); 7.97 (broad s, 2H); 7.65 (t, 1H, J=8.1 Hz); 4.08 (q, 2H, J=7.1 Hz); 1.11 (t, 3H, J=7.1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06962935B2
Source datasetuspto-grants-2005_11
ORD IDord-50334582c9e0479cb76d25cdb644e3ba
Source noteuspto-grants-2005_11