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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-(m-nitrophenyl)-3-oxopropionate | HCID 104078 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Hydroxy tosyloxy iodobenzene | HCID 21918218 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10447091 | HCID 10447091 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06962935B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-50334582c9e0479cb76d25cdb644e3ba |
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| Source note | uspto-grants-2005_11 |
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