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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694612Generated: November 1, 2026

Methyl trifluoromethyl ketone → HCID 178465586, compound

https://huagongshe.com/reaction/1694612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl trifluoromethyl ketoneHCID 9871—
Reactant3-Chloro-2-hydrazinylpyridineHCID 556100—
ReactantHCID 178514363HCID 178514363—
ProductHCID 178465586HCID 17846558666%

Reaction Steps

1,1,1-Trifluoroacetone (7.80 g, 69.6 mmol) was added to 3-chloro-2(1H)-pyridinone hydrazone (alternatively named (3-chloro-pyridin-2-yl)-hydrazine) (10 g, 69.7 mmol) at 20-25° C. After the addition was complete, the mixture was stirred for about 10 minutes. The solvent was removed under reduced pressure and the mixture partitioned between ethyl acetate (100 mL) and saturated aqueous sodium carbonate solution (100 mL). The organic layer was dried and evaporated. Chromatography on silica gel (eluted with ethyl acetate) gave the product as an off-white solid (11 g, 66% yield), mp. 64-64.5° C. (after crystallization from ethyl acetate/hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158802B2
Source datasetuspto-grants-2012_04
ORD IDord-640139f7cc704f0b9ad38a8462e68337
Source noteuspto-grants-2012_04