HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675306Generated: October 25, 2026
Potassium Carbonate → 5-(4-(Trifluoromethyl)phenyl)thiophene-2-carbaldehyde
https://huagongshe.com/reaction/1675306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromothiophene-2-carbaldehyde | HCID 78428 | — |
| Reactant | 4-(Trifluoromethyl)phenylboronic acid | HCID 2734389 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(4-(Trifluoromethyl)phenyl)thiophene-2-carbaldehyde | HCID 4674819 | 63% |
Reaction Steps
A mixture of 5-bromothiophene-2-carboxaldehyde 60.1 (1.03 g, 5.4 mmol), 4-(trifluoromethyl)benzeneboronic acid 61.1 (2.05 g, 10.9 mmol), K2CO3 (2.24 g, 16.2 mmol), and Pd(PPh3)4 (0.60 g, 0.54 mmol) in toluene (15 mL) was stirred for 5 Hours at 95° C. The mixture was cooled to room temperature, filtered through a pad of silica gel (EtOAc), and concentrated. The crude product was chromatographed on silica gel (0-30% EtOAc/hexane) to afford 61.2 (0.87 g, 63%) as off-white crystals. 1H NMR (400 MHz, CDCl3) δ 9.93 (s, 1H), 7.78 (m, 3H), 7.70 (d, 2H), 7.48 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003648B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-4654cd8c00724fb1a7dfcd410ee21c16 |
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| Source note | uspto-grants-2011_08 |
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