Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462050Generated: October 26, 2026

Phosphorus oxychloride → 2-(Methylthio)-5-(4-fluorobenzoyl)pyrrole

https://huagongshe.com/reaction/1462050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-fluoro-N,N-dimethylbenzamideHCID 141077—
ReactantSodium AcetateHCID 517045—
Reactant2-MethylthiopyrroleHCID 11007857—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product2-(Methylthio)-5-(4-fluorobenzoyl)pyrroleHCID 1291590154.4%

Reaction Steps

A solution of N,N-dimethyl-4-fluorobenzamide (8.4 g, 0.05 moles) in anhydrous 1,2-dichloroethane (170 ml) containing phosphorous oxychloride (7.7 g, 0.05 moles) was heated at reflux temperature for 1 hour. At the end of this time 2-methylthiopyrrole (2.82 g, 0.025 moles) was added and heating was continued for an additional 0.5 hour. The solution was cooled to room temperature, and to the cooled solution was cautiously added, with good agitation, a solution of sodium acetate (12.3 g, 0.15 moles) in water (50 ml) and the mixture was then boiled under reflux for 1 hour. The organic phase was separated, washed with water, dried, and evaporated. The residue was subjected to column chromatography on silica gel suing ethyl acetate-hexane (1:9) as the eluting solvent. A yellow colored solid 2-(methylthio)-5-(4-fluorobenzoyl)pyrrole (3.2 g, 54%) was obtained which after crystallization from ether-hexane had m.p. 112°-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04458081
Source datasetuspto-grants-1984_07
ORD IDord-edb1536751c348f5ab93ce525c913a46
Source noteuspto-grants-1984_07