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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963429Generated: October 30, 2026

N-(4-bromophenyl)-1,1,1-trifluoromethanesulfonamide → HCID 69993988, compound

https://huagongshe.com/reaction/963429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-bromophenyl)-1,1,1-trifluoromethanesulfonamideHCID 2133889—
ReactantEthylorthoformateHCID 53630039—
ProductHCID 69993988HCID 6999398893%

Reaction Steps

A solution of 1.52 g (5 mmol) of N-(4-bromophenyl)-C,C,C-trifluoro-methanesulphonamide (Example 13bv)) in 25 ml of ethyl orthoformate was heated to reflux for 6 hours. Subsequently, the readily volatile constituents were distilled off on a water-jet vacuum and the residue was chromatographed over a flash column with hexane/ethyl acetate 95:5. There were obtained 1.55 g (93%) of N-(4-bromophenyl)-N-ethyl-C,C,C- trifluoro-methanesulphonamide as a pale yellow oil. MS (EI): 331 and 333 (M+, 44%), 198 and 200 ([M-SO2 CF3 ]+, 80%), 118 ([M-(SO2CF3 +HBr)]+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763450
Source datasetuspto-grants-1998_06
ORD IDord-6d2ffc1f0a2c484785c08db57ee1fd57
Source noteuspto-grants-1998_06