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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590982Generated: October 29, 2026

Thiobenzamide → HCID 70818685, compound

https://huagongshe.com/reaction/590982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiobenzamideHCID 683563—
ReactantHCID 6504217HCID 6504217—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 70818685HCID 7081868594.1%

Reaction Steps

A solution of 2-chloro-1-(3,4-dihydro-2H-1-benzopyran-6-yl)ethan-1-one (9b) (250 mg, 1.19 mmol) and thiobenzamide (180 mg, 1.3 mmol) in dioxane (10 mL) was refluxed for 15 hours, then the reaction mixture was concentrated. The residue was diluted with dichloromethane (20 mL), washed with water (10 mL), brine (10 mL), dried over sodium sulfate, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (dichloromethane/cyclohexane 60/40) to afford the desired thiazole (9c) as a white solid (330 mg, 1.12 mmol, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-acad0a51e02441a9a5cd8cb33fa0541a
Source noteuspto-grants-2016_01