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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032908Generated: October 30, 2026

1,2-Dimethoxyethane → HCID 131718398, compound

https://huagongshe.com/reaction/1032908

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantAmmonium ChlorideHCID 25517—
Reactanto-(Trifluoromethyl)benzaldehydeHCID 123067—
Reactant2-Chloro-4-(trifluoromethyl)pyridineHCID 144958—
ReactantLithium diisopropylamideHCID 2724682—
ProductHCID 131718398HCID 131718398—

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a 3-neck flask equipped with a dropping funnel, a thermometer, and a condenser with a drying tube were added 5 grams of 2-chloro-4-trifluoromethyl pyridine and 5 ml of ethylene glycol dimethyl ether. The mixture was cooled to -70° C. and 22 ml of LDA were slowly added with the temperature maintained below -55° C. The reaction mixture was stirred at -70° C. for 1.5 hours, and 3.5 ml of 2-trifluoromethyl benzaldehyde added. The reaction mixture was stirred in a dry-ice bath, then at room temperature over night. Fifteen ml of saturated aqueous ammonium chloride solution was added, the solvent stripped and the oil residue washed with water and extracted with methylene chloride (3 times). The combined methylene chloride layers were washed with brine, dried and stripped to yield a brown oil. The brown oil was put onto a silica gel column and eluted with a 1:1 mixture of hexane and diethyl ether to yield 6.2 grams of 2-chloro-3-(1-hydroxy-2'-trifluoromethyl-benzyl)-4-trifluoro methyl-pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308826
Source datasetuspto-grants-1994_05
ORD IDord-a50b75cfa00e43cb8a4158b66b03efc0
Source noteuspto-grants-1994_05