HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259533Generated: October 30, 2026
Hydrogen Peroxide → 4-Chloro-3,5-difluoroaniline
https://huagongshe.com/reaction/2259533
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | 2,6-Difluoroaniline | HCID 79647 | — |
| Reactant | Benzene, 2-chloro-1,3-difluoro- | HCID 142257 | — |
| Reactant | 5-Bromo-2-chloro-1,3-difluorobenzene | HCID 2773258 | — |
| Reactant | 4-Chloro-3,5-difluorophenol | HCID 19436620 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 4-Chloro-3,5-difluoroaniline | HCID 19436621 | — |
Reaction Steps
Compound (250) can be prepared in the same manner as in Preparation Example 240, except for replacing compound (P102) with 4-chloro-3,5-difluorophenol. The 4-chloro-3,5-difluorophenol can be prepared by reacting a Grignard reagent prepared from 1-bromo-4-chloro-3,5-difluorobenzene with t-butyl hydroperoxide or converting the same Grignard reagent to a boric ester, and oxidizing the product with hydrogen peroxide under a basic condition. It is also prepared by nitrating 2-chloro-1,3-difluorobenzene (obtainable by decomposing a diazonium salt of 2,6-difluoroaniline in the presence of cuprous chloride or in hydrochloric acid), reducing the nitro-compound to obtain 4-chloro-3,5-difluoroaniline, and decomposing its diazonium salt in sulfuric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05474707 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-1d1a709b043a4d45a68f0961ea7e2b42 |
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| Source note | uspto-grants-1995_12 |
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