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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820837Generated: November 1, 2026

2-Bromoacetyl-6-methoxynaphthalene → HCID 68984203, compound

https://huagongshe.com/reaction/1820837

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromoacetyl-6-methoxynaphthaleneHCID 193452—
ReactantThiobenzamideHCID 683563—
SolventEthanolHCID 702—
ProductHCID 68984203HCID 6898420388.1%

Reaction Steps

Thiobenzamide (447 mg, 3.26 mmol) was added under nitrogen to a solution of (2-bromo-1-(6-methoxy-2-naphthyl)ethanone (906 mg, 3.25 mmol), prepared in the previous step, in 25 mL of absolute ethanol at approximately 70° C. After the addition the reaction was refluxed for 2 h. The solid was collected by filtration, rinsed with absolute ethanol and dried under reduced pressure to give 4-(6-methoxy-2-naphthyl)-2-phenyl-1,3-thiazole (909 mg, 88%) as a white solid, mp 191-193° C. Elemental Analysis for C20H15NOS Calc'd: C, 75.68; H, 4.76; N, 4.41. Found: C, 75.37; H, 4.65; N, 4.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605172B2
Source datasetuspto-grants-2009_10
ORD IDord-671a37ab098f4a5891058dad5542044e
Source noteuspto-grants-2009_10