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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536447Generated: October 30, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 89621236, compound

https://huagongshe.com/reaction/536447

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 68596223HCID 68596223—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89621236HCID 89621236—

Reaction Steps

A solution of Example 2B (7.75 g, 31.2 mmol) and THF (116 mL) was cooled to <5° C. and 1,8-diazabicyclo[5.4.0]undec-7-ene (7.91 mL, 53.0 mmol) and diphenylphosphoryl azide (10.09 mL, 46.8 mmol) were added. The yellow slurry was warmed slowly to ambient temperature, becoming a brown solution. After 14 hours, the mixture was concentrated, diluted with MTBE (200 mL), and washed with 2N NaOH (50 mL×2), brine (50 mL), 2N HCl (50 mL×2), and brine (50 mL). The organic layer was dried (Na2SO4), filtered, and concentrated to give the title compound. This material was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859584B2
Source datasetuspto-grants-2014_10
ORD IDord-52e11873f169414db595694861a28d38
Source noteuspto-grants-2014_10