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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (4-Chloro-2-fluoro-5-propan-2-yloxyphenyl)hydrazine | HCID 185080 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3,3-Dichloro-1,1,1-trifluoroacetone | HCID 2779020 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3,3,3-Trifluoro-2-oxopropanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone) | HCID 69141430 | 81.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06156891 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-d3871d39c0784dab8942e284a89243c4 |
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| Source note | uspto-grants-2000_12 |
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