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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267393Generated: October 31, 2026

4-Fluorobenzoyl chloride → (4-Fluorophenyl)-2-thiazolylmethanone

https://huagongshe.com/reaction/2267393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
Reactant2-TrimethylsilylthiazoleHCID 588453—
SolventDichloromethaneHCID 6344—
Product(4-Fluorophenyl)-2-thiazolylmethanoneHCID 275895677.9%

Reaction Steps

4-fluorobenzoyl chloride (3 mL, 25.4 mmol) was added to 2-(trimethylsilyl)thiazole (2 mL, 12.7 mmol) in dichloromethane (70 mL). The reaction mixture was stirred over night at rt. Dichloromethane was evaporated under reduced pressure, and the crude product purified on a normal phase silica-gel column with 0-40% ethyl acetate in hexane to afford the title compound as white amorphous solid (2.050 g, 77% yield); MS (M+H)+ 208.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-39c22c79ae9b4a3ab1cd2e8f25e943bf
Source noteuspto-grants-2010_12