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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740817Generated: November 3, 2026

Sodium hydride → HCID 21833674, compound

https://huagongshe.com/reaction/1740817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-BromothiazoleHCID 76430—
ReactantHCID 21833673HCID 21833673—
SolventDimethyl SulfoxideHCID 679—
SolventDimethylformamideHCID 6228—
ProductHCID 21833674HCID 2183367440.6%

Reaction Steps

To a mixture of 10 ml of anhydrous N,N-dimethylformamide and 110 mg of sodium hydride (60% oil dispersion) was added dropwise an anhydrous dimethylsulfoxide (5 ml) solution of 500 mg of 2-[4-(1-pyrazolyl)methylphenoxy]ethanol (produced in Reference Production Example 1 described below) under stirring over 10 minutes. After stirring at 60° to 70° C. for 2 hours, the mixture was cooled to 5° to 10° C., to which an anhydrous N,N-dimethylformamide (5 ml) solution of 488 mg of 2-bromothiazole was added dropwise over 10 minutes. The mixture was then stirred at room temperature overnight and then at 60° to 70° C. for further 2 hours. The reaction mixture was poured into 50 ml of ice water, which was extracted with twice with 30 ml of toluene. The organic layers were combined, washed with water, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, which afforded 280 mg of 4-(1-pyrazolyl)methylphenyl 2-(2-thiazolyloxy)ethyl ether (compound 5). Yield, 41%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972949
Source datasetuspto-grants-1999_10
ORD IDord-d29b8e6504fc433fa3bd3dc1e1c7c248
Source noteuspto-grants-1999_10