HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394778Generated: October 25, 2026
Ethyl benzoylacetate → Ethyl 2-amino-4-phenyl-1,3-thiazole-5-carboxylate
https://huagongshe.com/reaction/394778
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl benzoylacetate | HCID 7170 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Hydroxy tosyloxy iodobenzene | HCID 21918218 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 2-amino-4-phenyl-1,3-thiazole-5-carboxylate | HCID 73239 | 75.9% |
Reaction Steps
To a solution of ethyl 3-phenyl-3-oxopropionate (5.0 g, 26.0 mmol) in 100 mL of acetonitrile was added hydroxy(tosyloxy)iodobenzene (11.2 g, 28.6 mmol). The resulting suspension was stirred at 65° C. for 1 h at which time the reaction was a homogeneous solution. Thiourea (2.2 g, 28.6 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 4.9 g (70%) of the title compound as a yellow solid. 1H NMR (CDCl3) d 7.65 (m, 2H), 7.39 (m, 3H), 5.98 (broad s, 2H), 4.18 (q, 2H), 1.22 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06602895B2 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-0f7ec75b59b14721884206e1f615b0c5 |
|---|
| Source note | uspto-grants-2003_08 |
|---|