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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748007Generated: October 27, 2026

Dimethylformamide → 3-[2-(4-Fluorophenyl)oxazol-4-ylmethoxy]cyclohexanol

https://huagongshe.com/reaction/748007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1,3-CyclohexanediolHCID 10433—
ReactantSodium hydrideHCID 24758—
Reactant4-(Chloromethyl)-2-(4-fluorophenyl)-1,3-oxazoleHCID 16038260—
SolventTetrahydrofuranHCID 8028—
Product3-[2-(4-Fluorophenyl)oxazol-4-ylmethoxy]cyclohexanolHCID 21980291—

Reaction Conditions

Temperature25 °C

Reaction Steps

With ice-cooling, initially 2.25 g of an 80 percent suspension of sodium hydride and then 5.8 g of 1,3-cyclohexanediol were added to a mixture of 50 ml of dimethylformamide and 50 ml of tetrahydrofuran. The mixture was stirred at about 25° C. for 3 hours. 10.5 g of 4-chloromethyl-2-(4-fluorophenyl)oxazole (1) was then added, the mixture was heated at 70° C. and the reaction was monitored by thin-layer chromatography. After the reaction ended, the mixture was poured into ice-water and extracted with ethyl acetate. The organic phase was separated off, dried and concentrated and the residue was purified on silica gel by flash chromatography (ethyl acetate/n-heptane=1:1). This gave the alcohol 3 as an oil. C16H18FNO3 (291.33) MS(ESI): 292 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399777B2
Source datasetuspto-grants-2008_07
ORD IDord-770e3b4bf0854c4982335188246b756a
Source noteuspto-grants-2008_07