HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722923Generated: October 31, 2026
Sodium Hydroxide → 4-Chloro-2-fluoro-5-(2,2-difluorocyclopropylmethoxy)phenylhydrazine
https://huagongshe.com/reaction/1722923
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 4-Chloro-2-fluoro-5-(2,2-difluorocyclopropylmethoxy)aniline | HCID 14129432 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-2-fluoro-5-(2,2-difluorocyclopropylmethoxy)phenylhydrazine | HCID 14129435 | — |
Reaction Steps
29.3 g 4-Chloro-2-fluoro-5-(2,2-difluorocyclopropylmethoxy)aniline was treated first with 45 ml half concentrated hydrochloric acid and then with 273 ml concentrated hydrochloric acid. It was then cooled to -10° C. and treated dropwise with a solution of 8.3 g sodium nitrite in 17 ml water at a such rate that the temperature of the reaction mixture did not rise above -5° C. It was stirred for 3 hours at -5° C. and the at -15° C., a solution of tin (II) chloride dihydrate in 34 ml concentrated hydrochloric acid added dropwise at such a rate that the temperature of the reaction mixture did not exceed -10° C. It was warmed at room temperature overnight. For the work-up, it was cooled to 0° C. and slowly neutralised with with 430 ml 32% caustic soda solution. The precipitated tin hydroxide slurry was separated by filtration through Celite and the filter cake washed with ether and the aqueous mother liquor extracted with ether. The combined organic phases were dried over magnesium sulphate and the solvent removed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04859230 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-a929472749ed4e4ab58530842fd7faab |
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| Source note | uspto-grants-1989_08 |
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