HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419627Generated: October 25, 2026
2,6-Difluorobenzoyl isocyanate → Noviflumuron
https://huagongshe.com/reaction/1419627
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Difluorobenzoyl isocyanate | HCID 2733369 | — |
| Reactant | 3,5-Dichloro-2-fluoro-4-(1,1,2,3,3,3-hexafluoropropoxy)aniline | HCID 15404608 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | Noviflumuron | HCID 9828359 | 83.4% |
Reaction Steps
To a solution of 1.31 g 3,5-dichloro-2-fluoro-4-(1,1,2,3,3,3-hexafluoropropoxy) aniline in 5 mL 1,2-dichloroethane under an atmosphere of nitrogen at room temperature was added 0.87 g 2,6-difluorobenzoyl isocyanate dissolved in 10 mL dichloroethane dropwise over a 10 minute period. The mixture was stirred, warmed to 40° C. for a one hour period, then concentrated under vacuum to a brown solid 2.0 g. The mixture was chromatographed using a Michel-Miller low pressure silica gel column eluted with 4:1 dichloromethane/heptane. Like fractions were pooled and concentrated under vacuum to give 1.67 g of a light tan solid, mp 156°-7° C. Proton and 19F nmr spectra were consistent with the proposed structure. Anal. calcd C17H7Cl2F9N2O3 : C, 38.58; H, 1.33; N, 5.29. Found: C, 38.64; H, 1.40; N, 5.44.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05886221 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-517f917d2e8049cbb917c0d1735f693f |
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| Source note | uspto-grants-1999_03 |
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