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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399674Generated: October 31, 2026

Pyrrole-2-carboxaldehyde → HCID 19383047, compound

https://huagongshe.com/reaction/2399674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrole-2-carboxaldehydeHCID 13854—
ReactantSodium hydrideHCID 24758—
ReactantBenzene, 2-chloro-1-fluoro-4-(trifluoromethyl)-HCID 157153—
SolventDimethylformamideHCID 6228—
ProductHCID 19383047HCID 1938304755.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of pyrrole-2-carboxaldehyde (19.0 g, 0.2 mol) in N,N-dimethylformamide (50 ml) was added dropwise to a suspension of sodium hydride (80% dispersion in oil, 6.3 g, 0.21 mol) in N,N-dimethylformamide (100 ml), maintaining the temperature of the reaction between 5°-10° C. by means of ice-bath cooling. When the addition was complete, stirring was continued for 30 minutes, and then 3-chloro-4-fluorobenzotrifluoride (39.7 g, 0.20 mol) added. The mixture was stirred for 3 hours, then warmed to 50° C. for 18 hours. The mixture was cooled to room temperature and partitioned between diethyl ether and water. The ethereal extract was washed sequentially with water and brine, dried over magnesium sulfate, filtered and the filtrate evaporated. Trituration with hexane gave 1-(2'-chloro-4'-trifluoromethylphenyl)pyrrole-2-carboxaldehyde as a pale yellow solid (30.6 g), m.p. 119°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05451566
Source datasetuspto-grants-1995_09
ORD IDord-a3b19aa5a29e40eb81410bfd06d0a4b3
Source noteuspto-grants-1995_09