HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8395Generated: October 23, 2026
Sodium Chloride → 2-[2-(4-Fluorophenyl)ethenyl]-5-fluorobenzonitrile
https://huagongshe.com/en/reaction/8395
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | HCID 178418744 | HCID 178418744 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[2-(4-Fluorophenyl)ethenyl]-5-fluorobenzonitrile | HCID 54125122 | 23.2% |
Reaction Steps
Sodium hydride (60% in mineral oil; 1.66 g [0.993 g NaH], 1.4 mmol, 1.10 equiv) was added to a solution of diethyl-2-cyano-4-fluorobenzyl phosphonate (10.2 g-equiv, 37.6 mmol, 1.0 equiv) in DMF (40 mL) over a period of 2 min. The reaction was stirred for 20 min at room temperature. 4-Fluorobenzaldehyde (4.67 g, 38 mmol, 1.0 equiv) was then added over a period of 2 min. After stirring for 18 h, H2O (200 mL) and satd. NaCl (50 mL) were added and the resulting mixture was extracted with EtOAc (2×100 mL). The combined organic layers were washed with 1N NaOH (1×100 mL) and H2O (2×100 mL), dried (anhyd. Na2SO4), and rotary evaporated (>100° C., heat gun). The crude, dark-red crystalline/oil (7.49 g, 82.7%) was chromatographed twice on silica gel (50×250 mm, dry pack), eluting first with hexane/EtOAc [4:1] and the second chromatography with [30:1] to provide a TLC-pure, yellow compound (2.1 g, 23.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087765B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-b1ca4ad206c7491da2afea1c84001543 |
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| Source note | uspto-grants-2006_08 |
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