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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974073Generated: October 29, 2026

Trifluoromethanesulfonic anhydride → HCID 178506394, compound

https://huagongshe.com/reaction/974073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 19987724HCID 19987724—
SolventCfc 113HCID 6428—
ProductHCID 178506394HCID 17850639426.2%

Reaction Steps

Trifluoromethanesulfonic anhydride 176 microliters (1.05 mmol) was added to a solution of 300 mg (1.05 mmol) of 1-phenoxy-2-(trifluoromethylsulfinyl)benzene in 8 ml of 1,1,2-trichloro-1,2,2-trifluoroetane, and the mixture was stirred for 6 days at room temperature. The reaction solution was concentrated under reduced pressure. The residue was purified by silica gel thin-layer chromatography (acetonitrile:methylene chloride=1:3) to give 115 mg (26.2%) of S-(trifluoromethyl)dibenzo -1,4-oxathiinium trifluoromethanesulfonate as white crystals. The properties of the product are shown in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066795
Source datasetuspto-grants-1991_11
ORD IDord-f5e1b853748842be813e61d02315dd91
Source noteuspto-grants-1991_11