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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727907Generated: October 31, 2026

Sodium Hydroxide → HCID 15166265, compound

https://huagongshe.com/reaction/727907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 19600530HCID 19600530—
ReactantHCID 178527775HCID 178527775—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 15166265HCID 1516626579.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture comprising 1.0 g of [4-(2-phenoxyethoxy)-3-methylpyridine-2-yl]methanol, 0.60 ml of thionyl chloride and 12 ml of dichloromethane was kept at 40° C. for 60 minutes to carry out the reaction. The reaction mixture was distilled to remove the solvent. Thus, a brown syrupy residue was obtained. 50 ml of ethanol, 0.70 g of sodium hydroxide and 1.2 g of 2-mercaptobenzimidazole were added to the residue. The obtained mixture was heated at 70° C. for two hours and distilled to remove the ethanol. The obtained residue was chromatographed over a silica gel column and eluted with 30% ethyl acetate in hexane and then with ethyl acetate to obtain 1.2 g of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045552
Source datasetuspto-grants-1991_09
ORD IDord-019dfe692968485ab332d8f745e31eb0
Source noteuspto-grants-1991_09