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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507618Generated: November 2, 2026

(4-Fluorophenyl)-2-thiazolylmethanone → HCID 57428843, compound

https://huagongshe.com/reaction/507618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Fluorophenyl)-2-thiazolylmethanoneHCID 2758956—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
ProductHCID 57428843HCID 57428843—

Reaction Steps

A solution of (4-fluorophenyl)(thiazol-2-yl)methanone (1.05 g, 5.07 mmol) in diethyl ether (50 mL) and was cooled to 0° C., treated with methylmagnesium bromide (1.85 mL, 3.0 M in Et2O, 5.57 mmol) and stirred overnight at room temperature. The reaction was quenched with saturated ammonium chloride solution, extracted with diethyl ether (2×30 mL), washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to afford the title compound as an oily brown residue (1.052 g, 93% yield). MS (M+H)+ 224.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786132B2
Source datasetuspto-grants-2010_08
ORD IDord-2594214b9301450bb99e46ad53280127
Source noteuspto-grants-2010_08