HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109076Generated: November 1, 2026
2,4-Difluorophenyl isocyanate → HCID 10339996, compound
https://huagongshe.com/reaction/1109076
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Difluorophenyl isocyanate | HCID 593258 | — |
| Reactant | HCID 10421359 | HCID 10421359 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10339996 | HCID 10339996 | 32% |
Reaction Steps
Part C. A solution of the amine prepared in Part C (4.26 g, 18.6 mmol) in methylene chloride (20 mL) was cooled to 0° C., and a solution of 2,4-difluorophenyl isocyanate (2.20 mL, 18.6 mmol) in methylene chloride (20 mL) was added dropwise with stirring over 1 hour. After slow warming to ambient temperature over 18 hours, the reaction mixture was concentrated under vacuum, and the residual oil was purified by flash chromatography to afford N'-(2,4-difluorophenyl)-N-(3, 3-dimethyl-5-hydroxypentyl)-N-heptylurea as a colorless oil (2.31 g, 6.01 mmol, 32%). 1H NMR (CDCl3) δ 7.93(br q,1H,J=6.2 Hz); 6.89-6.78(m,3H); 3.76(t,2H,J=6.3 Hz); 3.38-3.24(m,4H); 2.36(br s,1H); 1.65-1.52(m,6H); 1.36-1.24(m,8H); 0.97(s,6H); 0.89(t,3H,J=6.6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05318984 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-f03313bef9f74b7b9afbaccc165a214a |
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| Source note | uspto-grants-1994_06 |
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