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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690692Generated: October 27, 2026

5-Oxo-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonate → HCID 16046965, compound

https://huagongshe.com/reaction/1690692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Oxo-5,6,7,8-tetrahydronaphthalen-2-yl trifluoromethanesulfonateHCID 11098384—
Reactant(4'-Butyl-biphenyl-3-yl)-hydrazine hydrochlorideHCID 66904838—
ProductHCID 16046965HCID 16046965—

Reaction Steps

The title material is prepared by reacting Trifluoro-methanesulfonic acid 5-oxo-5,6,7,8-tetrahydro-naphthalen-2-yl ester and (4′-Butyl-biphenyl-3-yl)-hydrazine hydrochloride (example 70, step 2) in an analogous manner and similar yield to example 1, step 3 except that purification is accomplished by reverse phase UV triggered HPLC. 1H NMR (400 MHz, d6-DMSO) d 11.63 (s, 1H), 7.78 (m, 2H), 7.58 (m, 4H), 7.46 (s, 1H), 7.33 (d, J=6.7 Hz, 1H), 7.28 (m, 2H), 3.09 (m, 2H), 2.95 (m, 2H), 2.64 (m, 2H), 1.60 (m, 2H), 1.35 (m, 2H), 0.94 (m, 3H); LC/MS calculated for [M+H]+ C27H25F3NO3S: 500.5, found: 500.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153671B2
Source datasetuspto-grants-2012_04
ORD IDord-48cc65cd0d3e4e35a0e2005cf2b59b32
Source noteuspto-grants-2012_04