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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334402Generated: October 29, 2026

Toluene → HCID 68276383, compound

https://huagongshe.com/reaction/334402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantHCID 68276473HCID 68276473—
SolventEthyl AcetateHCID 8857—
ProductHCID 68276383HCID 68276383106.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 3-amino-6-(3,5-difluorobenzylthio)picolinoamide (2.37 mmol, 0.7 g) and P2Cl5 (9.48 mmol, 1.346 g), 20 ml of toluene and 1 ml of ionic solvent (1-butyl-3-methylimidazolium tetrafluoroborate) are placed in a microwave reactor and then heated at 140° C. for 30 minutes. The crude reaction product is then concentrated under reduced pressure and the orange crystals thus obtained are redissolved in ethyl acetate and washed using saturated aqueous NaHCO3 solution. The organic phase is dried on magnesium sulfate and then concentrated to yield 0.7 g of a brown oil. This crude reaction product is purified by silica gel chromatography (AcOEt/heptane+0.1% of NEt3) to yield, after concentration, 0.15 g (23%) of orange crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883821B2
Source datasetuspto-grants-2014_11
ORD IDord-9dc689210e464efc9a353a163df85984
Source noteuspto-grants-2014_11