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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32104Generated: October 26, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → Trifluoromethanesulfonic acid 5-azido-5,6,7,8-tetrahydronaphthalen-2-yl ester

https://huagongshe.com/reaction/32104

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantTrifluoromethanesulfonic acid 5-hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 72440636—
SolventTetrahydrofuranHCID 8028—
ProductTrifluoromethanesulfonic acid 5-azido-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 72440623—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of trifluoro-methanesulfonic acid 5-hydroxy-5,6,7,8-tetrahydro-naphthalen-2-yl ester (Step B, 11.2 g, 37.9 mmol, 1.0 eq) in THF (150 mL) at RT was added DPPA (Aldrich, 11.1 mL, 51.6 mmol, 1.36 eq). The resulting mixture was cooled to 0° C. and then DBU (Aldrich, 7.7 mL, 51.6 mmol, 1.36 eq) was added slowly through a syringe. The reaction was warmed to RT and stirred over the weekend. The mixture was concentrated in vacuo. The residue was dissolved in EtOAc (400 mL), washed with saturated NH4Cl (twice), H2O, and brine, dried over Na2SO4 and concentrated in vacuo. The crude was purified by flash chromatography (5% EtOAc-hexane) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425631B2
Source datasetuspto-grants-2008_09
ORD IDord-3067549d00b343a99b3b01aebcad077a
Source noteuspto-grants-2008_09