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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450858Generated: October 26, 2026

Benzyltrimethylammonium hydroxide → HCID 178510368, compound

https://huagongshe.com/reaction/450858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant2-CyanoethanethioamideHCID 1416277—
ReactantSodiumHCID 5360545—
Reactant2-Dimethoxymethyl-3-hydroxy-acrylonitrileHCID 57937103—
SolventHydrochloric AcidHCID 313—
SolventTriethylamineHCID 8471—
ProductHCID 178510368HCID 178510368—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of the sodium salt of 2-dimethoxymethyl-3-hydroxy-acrylonitrile (3.94 g, 23.86 mmol) in hydrochloric acid (20 ml, 0.5 M) is heated at 50° C. for 30 minutes. Excess hydrochloric acid is neturalized using triethylamine, before adding cyanoacetothioamide (2.39 g, 23.9 mmol) and a catalytic amound of benzyltrimethylammonium hydroxide. The mixture is stirred at room temperature for two hours, heated at 60° C. for 2 hours and then refluxed for 4 hours. Evaporation of the solvents leaves a solid that is purified on silicagel to yield 3,5-dicyano-2-marcaptopyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486996B2
Source datasetuspto-grants-2013_07
ORD IDord-0704176d76584d41a772a9f45bc0554a
Source noteuspto-grants-2013_07