HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371269Generated: October 31, 2026
4-Nitrophenethyl alcohol → 1-(2-Fluoroethyl)-4-nitrobenzene
https://huagongshe.com/reaction/1371269
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenethyl alcohol | HCID 7494 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Fluoroethyl)-4-nitrobenzene | HCID 14809007 | — |
Reaction Steps
A solution of 2-(4-nitrophenyl)ethanol (835 mg) in methylene chloride (30 mL) was stirred at −78° C. under a nitrogen atomosphere. To this solution, diethylaminosulfur trifluoride (1.98 mL) in methylene chloride (20 mL) was added dropwise over 10 minutes. With stirring, the temperature of the reaction mixture was allowed to rise back to room temperature. After 30 minutes, the reaction was stopped by the addition of saturated aqueous sodium hydrogen carbonate solution (50 mL) in an ice bath. The methylene chloride solution was washed with saturated aqueous sodium hydrogen carbonate solution (50 mL). After drying over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure. The residue was purified by chromatography on a silica gel (25 g) column using hexane:ethyl acetate (7:2) as the eluant to give 1-fluoro-2-(4-nitrophenyl)ethane (359 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157442B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-797e93aa1ccb49db8a3e3ff7a245dcc9 |
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| Source note | uspto-grants-2007_01 |
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