Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787734Generated: October 30, 2026

Methyl iodide → HCID 57825894, compound

https://huagongshe.com/reaction/1787734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHydrazineHCID 9321—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(4-Bromo-2-hydroxyphenyl)ethan-1-oneHCID 10727403—
SolventAcetoneHCID 180—
ProductHCID 57825894HCID 578258941.4%

Reaction Steps

Methyl iodide (3 mL, 47.3 mmol) was added to a solution of 4-bromo-2-hydroxyacetophenone (9.25 g, 43 mmol) and potassium carbonate (6.54 g, 47.3 mmol) in acetone (20 mL) and the mixture was stirred at room temperature for 18 hours. The reaction mixture was concentrated in vacuo to low volume and diluted with water. The aqueous mixture was extracted with dichloromethane (3×50 mL) and the combined organic solution was washed with water, dried over sodium sulfate and concentrated in vacuo. The residue was dissolved in 1,2-ethanediol (10 mL), hydrazine (19.47 mL, 400 mmol) and potassium hydroxide (7.86 g, 140 mmol) were added and the reaction mixture was heated at 150° C. for 60 hours. The reaction mixture was then quenched with 1M hydrochloric acid and extracted with ethyl acetate (3×20 mL). The combined organic solution was dried over sodium sulfate, concentrated in vacuo and the residue was purified by Kugel Rohr fractional distillation (150° C./0.05 mbar) to provide the title compound as a yellow oil (128 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511057B2
Source datasetuspto-grants-2009_03
ORD IDord-9978c40cf11d4fc6912e32bd90f6e968
Source noteuspto-grants-2009_03