HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399674Generated: October 31, 2026
Pyrrole-2-carboxaldehyde → HCID 19383047, compound
https://huagongshe.com/reaction/2399674
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrole-2-carboxaldehyde | HCID 13854 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzene, 2-chloro-1-fluoro-4-(trifluoromethyl)- | HCID 157153 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19383047 | HCID 19383047 | 55.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05451566 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-a3b19aa5a29e40eb81410bfd06d0a4b3 |
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| Source note | uspto-grants-1995_09 |
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