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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013458Generated: October 31, 2026

Trifluoromethylsulfonamide → HCID 57925961, compound

https://huagongshe.com/reaction/1013458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethylsulfonamideHCID 79001—
ReactantHCID 57925832HCID 57925832—
SolventDimethylformamideHCID 6228—
ProductHCID 57925961HCID 57925961—

Reaction Steps

4-(1-Methyl-4-oxido-1,4-azaphosphinan-4-yl)phenol (0.50 g, 2.22 mmol) was made 0.5 M in DMF and N-Phenyl-bis(trifluorometanesulfonamide (1.19 g, 3.33 mmol) was added, followed by TEA (0.62 mL, 4.44 mmol). The mixture was stirred at ambient temperature for 16 h then the precipitate was filtered off and the filtrate was concentrated in vacuo. The residue was purified by HPLC (20-95% MeCN in water w/0.025% TFA). Pure fractions were identified, combined and concentrated in vacuo. The residue was taken up in EtOAc and washed with saturated aqueous sodium bicarbonate (1×) then dried (MgSO4) and concentrated in vacuo to afford the requisite product as a freebase. MS: cal'd 358 (MH+), exp 358 (MH

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981874B2
Source datasetuspto-grants-2011_07
ORD IDord-385f3c369d0145a5b575ad599404b297
Source noteuspto-grants-2011_07