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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931124Generated: October 31, 2026

Methyl triflate → HCID 178480273, compound

https://huagongshe.com/reaction/1931124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl triflateHCID 9526—
ReactantAmmonium HydroxideHCID 14923—
Reactantn-[3-Tert-butyl-1-(4,4,4-trifluorobutyl)-1h-pyrazol-5-yl]-2-fluoro-5-(trifluoromethyl)benzamideHCID 87087570—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 178480273HCID 17848027374.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of Example 135C (1.7 g, 3.9 mmol) in toluene (15 mL) was added methyl trifluoromethanesulfonate (0.64 mL, 5.8 mmol). The mixture was warmed to 100° C. and stirred for 20 hours, cooled to ambient temperature and diluted with water (20 mL) and acetone (50 mL). This solution was allowed to stir for 30 minutes then concentrated NH4OH (10 mL) was added. The mixture was stirred for 30 minutes then partially concentrated under reduced pressure. The mixture was diluted with EtOAc (30 mL) and brine (10 mL) and the layers were separated. The aqueous phase was extracted with EtOAc (3×5 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification by column chromatography (SiO2, 80% hexanes/EtOAc to 100% EtOAc to 10% MeOH in EtOAc) afforded the title compound (1.3 g, 2.9 mmol, 74% yield). MS (ESI−) m/z 454 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188135B2
Source datasetuspto-grants-2012_05
ORD IDord-279903aeaa99497e8c1978e16a379b57
Source noteuspto-grants-2012_05