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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935442Generated: October 27, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 22464525, compound

https://huagongshe.com/reaction/1935442

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-(2,2,2-Trifluoroethoxy)-5-chlorobenzyl alcoholHCID 43141932—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22464525HCID 22464525—

Reaction Steps

To a solution of 2-(2,2,2-trifluoroethoxy)-5-chlorobenzyl alcohol (1.9 g, 7.9 mmol) in THF (20 mL) at 0° C. was added diphenyl phosphoryl azide (2.2 mL, 10.2 mmol) followed by DBU (1.5 mL, 10.0 mmol). The reaction mixture was allowed to warm to room temperature overnight following which the solvent was removed under reduced pressure. The residue was partitioned between ether and water and the organic layer dried over sodium sulfate. Filtration, concentration and purification by flash chromatography (19:1 hexane/ether) gave the azide as a white solid: 1H NMR (CDCl3) δ7.31 (m, 2H), 6.82 (d, J=8.8 Hz, 1H), 4.40 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387911B1
Source datasetuspto-grants-2002_05
ORD IDord-0f2609cb8b0e478e8a6dcf6e57f9fb41
Source noteuspto-grants-2002_05