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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500686Generated: October 29, 2026

Azide → HCID 57443977, compound

https://huagongshe.com/reaction/500686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzideHCID 33558—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 57443976HCID 57443976—
SolventTolueneHCID 1140—
ProductHCID 57443977HCID 5744397780.4%

Reaction Steps

To a solution of ethyl 6-(1-hydroxyethyl)-1-benzothiophene-2-carboxylate (2.0 g, 8.06 mmol) in toluene (30 mL) was added diphenylphosphorylazide (2.64 g, 9.58 mmol), then DBU (1.31 mL, 8.79 mmol) dropwise. After 24 h, added more azide (0.5 mL) and DBU (0.3 mL) to the thick solution. After an additional 24 h, the reaction mixture was concentrated and purified via column chromatography yielding the desired product (1.77 g, 80.4% over two steps). 1H NMR (CDCl3, 600 MHz) δ 8.03 (d, J=0.9 Hz, 1H), 7.87 (d, J=8.2 Hz, 1H), 7.81 (m, 1H), 7.36 (dd, J=8.2, 0.9 Hz, 1H), 4.75 (q, J=6.8 Hz, 1H), 4.40 (q, J=7.3 Hz, 2H), 1.58 (d, J=6.8 Hz, 3H), 1.41 (t, J=7.3 Hz, 3H). MS: cal'd 276 (MH+), exp 276 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772238B2
Source datasetuspto-grants-2010_08
ORD IDord-c9e397420c034d1ab17295d3ddb04d82
Source noteuspto-grants-2010_08