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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045831Generated: October 31, 2026

N-methyl-N-phenyl-hydrazine → HCID 58256489, compound

https://huagongshe.com/reaction/2045831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-N-phenyl-hydrazineHCID 36299—
Reactant1-Chloro-3-(4-fluorophenyl)hex-5-en-3-olHCID 53472938—
CatalystTetrabutylammonium IodideHCID 67553—
ProductHCID 58256489HCID 582564897.6%

Reaction Conditions

Temperature63 °C

Reaction Steps

1-chloro-3-(4-fluorophenyl)hex-5-en-3-ol (58 mg, 0.25 mmol), 1-methyl-1-phenylhydrazine (500 mg, 4.09 mmol), and tetrabutylammonium iodide (92 mg, 0.25 mmol) were combined and heated in a microwave for 50 min at 63° C. The crude mixture was filtered and purified twice by chromatography on a silica gel cartridge eluted with an EtOAc/hexanes gradient to remove 1-methyl-1-phenylhydrazine. The residue was dissolved in Et2O and washed with 1 M aq HCl. The aqueous layer was treated with 1 M aq NaOH until a pH of 4 was reached, then extracted with Et2O. The organic layer was evaporated and the residue was further purified by preparative HPLC to provide 3-(4-fluorophenyl)-1-(2-methyl-2-phenylhydrazinyl)hex-5-en-3-ol (6 mg). LC-MS Method 1 m/z=315 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592409B2
Source datasetuspto-grants-2013_11
ORD IDord-4ed7b5b07172425f9061693c55d32649
Source noteuspto-grants-2013_11