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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591563Generated: October 26, 2026

Tributylphosphine → Methyl(4-fluoro-6-((1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)methoxy)-1-benzothiophen-3-yl)acetate

https://huagongshe.com/reaction/591563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant(1-Methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)methanolHCID 58456726—
ReactantMethyl(4-fluoro-6-hydroxy-1-benzothiophen-3-yl)acetateHCID 129359611—
SolventTetrahydrofuranHCID 8028—
ProductMethyl(4-fluoro-6-((1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)methoxy)-1-benzothiophen-3-yl)acetateHCID 11866706674.2%

Reaction Steps

To a mixture of tri-n-butylphosphine (0.793 mL), (1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)methanol (187 mg), methyl(4-fluoro-6-hydroxy-1-benzothiophen-3-yl)acetate (250 mg) and THF (dry) (15 mL) was added ADDP (801 mg) at room temperature. The mixture was stirred at room temperature for 2 h and then concentrated in vacuo. To the residue was added IPE and the insoluble materials were removed by filtration. The filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography (NH, EtOAc/hexane) and silica gel column chrothatography (EtOAc/hexane) to give the title compound (310 mg). The crystals were recrystallized from acetone-hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-f73cf3400212418c9d87da9c4c09feab
Source noteuspto-grants-2016_01