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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255822Generated: October 30, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-[(1S)-1-azidoethyl]-3-nitrobenzene

https://huagongshe.com/reaction/1255822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant(R)-1-(3-nitrophenyl)ethanolHCID 11147933—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-[(1S)-1-azidoethyl]-3-nitrobenzeneHCID 86641855130.1%

Reaction Steps

To a solution of (1R)-1-(3-nitrophenyl)ethanol (12 g, 72 mmol) in tetrahydrofuran (220 mL), cooled to 0° C., was added diphenylphosphoryl azide (31 mL, 145 mmol) in one portion followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (22 mL, 145 mmol) dropwise over 30 minutes. The reaction mixture was allowed to warm slowly to room temperature and was stirred for 38 hours after which time the mixture was diluted with ethyl acetate (100 mL) and water (100 mL), the two phases separated and the aqueous phase extracted with ethyl acetate (2×100 mL). The combined organic phases were washed with brine (100 mL), dried (MgSO4) and concentrated under reduced pressure to give a black liquid. The crude liquid was purified by flash chromatography (silica, ethyl acetate/hexanes) to give 1-[(1S)-1-azidoethyl]-3-nitrobenzene (18 g) as a yellow liquid in acceptable purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461161B2
Source datasetuspto-grants-2013_06
ORD IDord-8fb5db18e66447ec93f3327bc56d3e98
Source noteuspto-grants-2013_06