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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090318Generated: October 30, 2026

3-(Trifluoromethyl)benzyl chloride → HCID 178506164, compound

https://huagongshe.com/reaction/1090318

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzyl chlorideHCID 69716—
ReactantSodiumHCID 5360545—
ReactantHCID 178527813HCID 178527813—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 178506164HCID 178506164—

Reaction Steps

To a solution of 0.15 g (0.0065 g atom) of sodium in 35 mL of methanol was added 1.0 g (0.0066 mol) of 2-mercapto-1H-imidazo[4,5-c]pyridine. After stirring for 15 minutes at room temperature, the methanol was removed in a rotary evaporator. The residue was dissolved in 20 mL of DMF and 1.28 g (0.0066 mol) of α'-chloro-α,α,α-trifluoro-m-xylene in 2 mL of DMF was added dropwise to the reaction solution. The reaction mixture was stirred at room temperature overnight and was then poured into 150 mL of ice water. The product which crystallized was collected and amounted to 1.61 g. An analytical sample (m.p. 148°-150° C.) was obtained by recrystallization from acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081253
Source datasetuspto-grants-1992_01
ORD IDord-b58604d9a94d4ca5a075bda3fcbcee19
Source noteuspto-grants-1992_01