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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909848Generated: October 26, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → Ethyl 5-(1-azidoethyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/1909848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantEthyl 5-(1-hydroxyethyl)thiophene-2-carboxylateHCID 59355961—
SolventTolueneHCID 1140—
ProductEthyl 5-(1-azidoethyl)thiophene-2-carboxylateHCID 5830671390.7%

Reaction Steps

To a mixture of ethyl 5-(1-hydroxyethyl)thiophene-2-carboxylate (1.01 g), diphenylphosphorylazide (1.67 g), and toluene (10 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (905 μL) under ice-cooling, followed by stirring for 30 minutes. The reaction mixture was warmed to room temperature, followed by stirring for 15 hours. The reaction liquid was washed with water and 1 M hydrochloric acid in this order, and dried over anhydrous sodium sulfate. Then, after concentration under reduced pressure, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain ethyl 5-(1-azidoethyl)thiophene-2-carboxylate (1.03 g) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598355B2
Source datasetuspto-grants-2013_12
ORD IDord-9544ac1f4e64428db0630cf4b0de3529
Source noteuspto-grants-2013_12