HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756904Generated: October 30, 2026
2,4-Difluorophenyl isocyanate → HCID 10206258, compound
https://huagongshe.com/reaction/1756904
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Difluorophenyl isocyanate | HCID 593258 | — |
| Reactant | HCID 21469551 | HCID 21469551 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 10206258 | HCID 10206258 | — |
Reaction Steps
The compound from (a) above (1.5 g; 4.5 mmoles) was dissolved in tetrahydrofuran (20 mL), cooled to -20° C., and then treated dropwise with n-butyllithium (2.8 mL; 4.5 mmoles) for over 5 minutes. The solution was stirred for 5 minutes before adding 2,4-difluorophenyl isocyanate (0.7 g; 4.5 mmoles). The ice bath was removed and the solution gradually warmed to room temperature over 30 minutes, at which time the reaction was quenched with water (20 mL) and diluted with ethyl acetate. The layers were separated and the organic portion was washed with aqueous HCl (1N), aqueous sodium carbonate (10%), and brine. The solution was dried over magnesium sulfate, filtered, and stripped to dryness leaving a viscous liquid that was dissolved in 75% hexane/25% ethyl acetate and chromatographed using silica gel. Yield: 0.9 g (41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05441975 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-43f71793528e40509f27818a841734de |
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| Source note | uspto-grants-1995_08 |
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