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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantStannous chloride dihydrateHCID 61436—
Reactant4-Chloro-2-fluoro-5-(2,2-difluorocyclopropylmethoxy)anilineHCID 14129432—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product4-Chloro-2-fluoro-5-(2,2-difluorocyclopropylmethoxy)phenylhydrazineHCID 14129435—

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859230
Source datasetuspto-grants-1989_08
ORD IDord-a929472749ed4e4ab58530842fd7faab
Source noteuspto-grants-1989_08