HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822146Generated: November 1, 2026
Phosphorus oxychloride → HCID 68980960, compound
https://huagongshe.com/reaction/1822146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3,4-Difluoro-2-(3,5-bis-tert-butylcarbamoyl-phenoxy)nitrobenzene | HCID 68981237 | — |
| Product | HCID 68980960 | HCID 68980960 | — |
Reaction Steps
In another embodiment of the present invention there is provided a process for the preparation of a compound according to formula III wherein R2 is 3,5-dicyano-phenyl which process further comprises (i) contacting sodium 3,5-bis-tert-butylcarbamoyl-phenolate with 2,3,4-trifluoronitrobenzene in an appropriate solvent at temperatures from about −30° C. up to about 40° C. to afford a 3,4-difluoro-2-(3,5-bis-tert-butylcarbamoyl-phenoxy)nitrobenzene; and (ii) contacting 3,4-difluoro-2-(3,5-bis-tert-butylcarbamoyl-phenoxy)nitrobenzene with phosphorus oxychloride or a similar dehydrating agent to afford 3,4-difluoro-2-(3,5-dicyano-phenoxy)nitrobenzene 111 (R2=3,5-dicyanophenyl). The ether can be convert to IV (R2=3,5-dicyanophenyl) as described below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608731B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-3a0324b0ee934cc8a4cfc60c3cfbeb74 |
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| Source note | uspto-grants-2009_10 |
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