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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl benzoylacetateHCID 7170—
ReactantThioureaHCID 2723790—
ReactantHydroxy tosyloxy iodobenzeneHCID 21918218—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-amino-4-phenyl-1,3-thiazole-5-carboxylateHCID 7323975.9%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06602895B2
Source datasetuspto-grants-2003_08
ORD IDord-0f7ec75b59b14721884206e1f615b0c5
Source noteuspto-grants-2003_08