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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207962Generated: November 1, 2026

Hydrazine, (4-chlorophenyl)-, hydrochloride (1:1) → HCID 118431820, compound

https://huagongshe.com/reaction/2207962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
ReactantHCID 131735937HCID 131735937—
SolventAcetic AcidHCID 176—
ProductHCID 118431820HCID 11843182060.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

4,4,5,5,5-Pentafluoro-1-(4′-methylsulfanyl-biphenyl-3-yl)-pent-1-en-3-one (200.0 mg, 0.54 mmol) prepared in Step 3 of Preparation 4 and 4-chlorophenylhydrazine hydrochloride (106.0 mg, 0.59 mmol) were added to acetic acid (3.0 mL). The reaction mixture was stirred at 120° C. for 8 hours, concentrated under reduced pressure, and then ethyl acetate was added thereto. The reaction mixture was washed with a saturated solution of sodium hydrogen carbonate, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a yellow liquid residue. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/60) to give 163.0 mg of the titled compound as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-18d1580a7b3b4ed29741cd0c4c8cac15
Source noteuspto-grants-2016_06