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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399012Generated: October 30, 2026

Acetonitrile → HCID 73676527, compound

https://huagongshe.com/reaction/2399012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 54247884HCID 54247884—
ReactantHCID 86734772HCID 86734772—
SolventPyridineHCID 1049—
ProductHCID 73676527HCID 7367652735%

Reaction Steps

Phosphoryl chloride (1.0 ml) is added to a stirred suspension of 1,3-Bis(1-methyl-2-(1H)-quinolylidene)acetone (0.68 g, 0.002 mol) in pyridine (10 ml). The mixture is stirred for 5 min., then the solid is collected and washed with a little pyridine, then with ether. The dye is converted to its perchlorate salt by solution in methanol, followed by addition of aqueous sodium perchlorate solution. After recrystallization from acetonitrile, the yield of purified dye is 0.30 g (36%) with the melting point indistinct. The following two dyes were prepared by procedures similar to that described above: 1,3-Diethyl-2-[(1,3-diethyl-1H-imidazo[4,5-b]quinoxalin-2-(3H)-ylidene)-1-propynyl]-1H-imidazo[4,5-b]quinoxalinium perchlorate. ##STR20##Recrystallized from acetonitrile. Purified yield 35%. mp > 300°. 1,3,3-Trimethyl-2-[(1,3,3-trimethyl-2-indolinylidene)-1-propynyl]-3H-indolium perchlorate. ##STR21##Recrystallized from methanol. Purified yield 43% mp 194°-7° dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04026884
Source datasetuspto-grants-1977_05
ORD IDord-3e9aad2977ce46b4b2e8cd1d780071d9
Source noteuspto-grants-1977_05