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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097822Generated: November 1, 2026

4-Methylthiazole → HCID 66811276, compound

https://huagongshe.com/reaction/1097822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylthiazoleHCID 12748—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66811276HCID 6681127616.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 4-methylthiazole (4.0 g, 40.33 mmol) in THF (80 mL) was cooled to −78° C. under nitrogen. n-Butyl lithium (20.4 mL of 2M in hexanes, 40.8 mmol) was added to the reaction mixture slowly over 3 minutes. The reaction mixture was stirred for about 1.5 hours at −78° C., and then 2-fluoronitrobenzene (6.24 g, 44.23 mmol) was added. After stirring at −78° C. for another 30 minutes, the reaction mixture was allowed to warm to room temperature. The reaction mixture was stirred for about 2 hours at room temperature and then the reaction was quenched with water (70 mL). The mixture was extracted with ethyl acetate and the combined organic layers were washed with brine (10 mL), dried (MgSO4), filtered and concentrated. The product was isolated by silica gel chromatography (5-10% ethyl acetate in hexanes) to give the title compound as an orange/brown oil (1.5 g). MS m/z: [M+H+] calcd for C10H8N2O2S 221.03; found 221. Retention time (HPLC 2-90)=4.54

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143277B2
Source datasetuspto-grants-2012_03
ORD IDord-0c7b9594c0b84739affedac90ea4958e
Source noteuspto-grants-2012_03