Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460592Generated: October 29, 2026

Water → HCID 135794325, compound

https://huagongshe.com/reaction/460592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethylhydrazineHCID 6061—
Reactant1-(4-Methoxy-2-benzofuranyl)-1,3-butanedioneHCID 22728976—
SolventMethanolHCID 887—
ProductHCID 135794325HCID 13579432586.5%

Reaction Conditions

Temperature-40 °C

Reaction Steps

1-(4-Methoxybenzo(b)furan-2-yl)butan-1,3-dione (1.0 g) was dissolved in methanol (30 ml) and methylhydrazine (0.3 g) was added thereto. The mixture was refluxed under heating for 20 min. The reaction solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/acetone). To the obtained oil was added methylene chloride (30 ml), and the mixture was cooled to −40° C., and boron tribromide (1 ml) was added dropwise. After the completion of the reaction, the mixture was poured into water and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and after filtration, the solvent was evaporated under reduced pressure to give 3-(4-hydroxybenzo(b)furan-2-yl)-1,5-dimethylpyrazole (0.85 g) as a brown oil. Using this and (S)-glycidyl nosylate (0.75 g) and in the same manner as in Starting Material Synthesis Example 1, the title compound (0.53 g) was obtained as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196199B2
Source datasetuspto-grants-2007_03
ORD IDord-f21139ea4be74816bac144a55872fa99
Source noteuspto-grants-2007_03