HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718019Generated: October 29, 2026
4-(Trifluoromethyl)benzaldehyde → HCID 15667942, compound
https://huagongshe.com/reaction/718019
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Trifluoromethyl)benzaldehyde | HCID 67996 | — |
| Reactant | 1-Pentene, 5-bromo- | HCID 70704 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15667942 | HCID 15667942 | — |
Reaction Steps
A mixture of 5-bromopent-1-ene (6.0 g, 40 mmol) and magnesium (1.44 g, 59.2 mmol) in tetrahydrofuran (40 mL) was stirred at 0° C. for 30 minutes. 4-(Trifluoromethyl)benzaldehyde (4.6 g, 26 mmol) was added drop-wise, and the reaction mixture was stirred at room temperature for 4 hours, then quenched by addition of water (30 mL). After extraction with ethyl acetate (3×15 mL), the combined organic layers were washed with saturated aqueous sodium chloride solution (10 mL), dried over sodium sulfate, filtered, and concentrated in vacuo to afford the product as a yellow oil. This was used without additional purification. Yield: 2.6 g, 11 mmol, 42%. 1H NMR (400 MHz, CDCl3) δ 7.58-7.64 (m, 2H), 7.44-7.50 (m, 2H), 5.72-5.84 (m, 1H), 4.93-5.04 (m, 2H), 4.73-4.79 (m, 1H), 2.05-2.13 (m, 2H), 1.64-1.85 (m, 2H), 1.47-1.60 (m, 1H), 1.34-1.47 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193726B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-4ecd5973f9ca47c39580aa8841c5b9a7 |
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| Source note | uspto-grants-2015_11 |
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