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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274513Generated: October 27, 2026

(4-Chloro-2-fluoro-5-propan-2-yloxyphenyl)hydrazine → 3,3,3-Trifluoro-2-oxopropanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone)

https://huagongshe.com/reaction/1274513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chloro-2-fluoro-5-propan-2-yloxyphenyl)hydrazineHCID 185080—
ReactantSodium AcetateHCID 517045—
Reactant3,3-Dichloro-1,1,1-trifluoroacetoneHCID 2779020—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product3,3,3-Trifluoro-2-oxopropanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone)HCID 6914143081.8%

Reaction Steps

To a solution of 5.3 g of sodium acetate dissolved in 100 ml of water was added 4.4 g of 1,1-dichloro-3,3,3-trifluoroacetone under ice cooling, and the reaction was allowed to proceed at 90° C. for 30 minutes. The reaction solution was left cooling to room temperature, to which a solution of 5.8 g of 2-fluoro-4-chloro-5-isopropoxyphenylhydrazine dissolved in 20 ml of diethyl ether was added, and the mixture was stirred at room temperature for 1 hour. The organic layer was separated, washed once with 10 ml of saturated aqueous sodium chloride solution, dried with anhydrous magnesium sulfate, and evaporated to remove the diethyl ether to give 6.5 g of 3,3,3-trifluoro-2-oxopropanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone), compound 3-3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156891
Source datasetuspto-grants-2000_12
ORD IDord-d3871d39c0784dab8942e284a89243c4
Source noteuspto-grants-2000_12