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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097534Generated: November 1, 2026

Tetrahydrofuran → HCID 66810289, compound

https://huagongshe.com/reaction/1097534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 66810464HCID 66810464—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 66810289HCID 6681028987.7%

Reaction Steps

To a solution of methyl 2-[4-fluoro-3-({[3-(trifluoromethyl)phenyl]acetyl}amino)phenoxy]-5-nitrobenzoate (3.75 g, 7.62 mmol) in methanol (40 mL)/tetrahydrofuran (8 mL) solution was added 10% palladium-carbon (400 mg), and the mixture was stirred at room temperature for 6 hr under a hydrogen atmosphere (1 atm). Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (ethyl acetate/n-hexane=30/70→80/20), and the fraction containing the object product was concentrated under reduced pressure to give the title compound (3.09 g, 87%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143258B2
Source datasetuspto-grants-2012_03
ORD IDord-94dc8fb78e3a452a9853cd460e9f1cd4
Source noteuspto-grants-2012_03