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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196498Generated: November 1, 2026

Di-tert-butyl azodicarboxylate → Di-tert-butyl 1-(5-formylthiophen-3-yl)hydrazine-1,2-dicarboxylate

https://huagongshe.com/reaction/2196498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant2-Formylthiophene-4-boronic acidHCID 11084115—
CatalystCupric acetateHCID 8895—
SolventTetrahydrofuranHCID 8028—
ProductDi-tert-butyl 1-(5-formylthiophen-3-yl)hydrazine-1,2-dicarboxylateHCID 5984328986%

Reaction Steps

To a solution of 5-formylthiophen-3-ylboronic acid (2 g, 12.82 mmol) and di-tert-butyl azodicarboxylate (1.476 g, 6.41 mmol) in THF (12 mL) under nitrogen was added copper(II) acetate (0.116 g, 0.641 mmol) in one portion according to the procedure of T. Uemura and N. Chatani (J. Org. Chem. 2005, 70, 8631-8634). The suspension was then stirred for 18.5 hours at room temperature. The resulting brown solution was then concentrated and the residue was dissolved in DCM and methanol and loaded on silica and applied to a 40M Biotage column. Elution with a gradient of 10 to 20% ethyl acetate in hexanes gave compound 11 (1.888 g, 86%) as a yellow crust. LRMS (ESI): calc. 342.12; found 365.2 (MNa)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338437B2
Source datasetuspto-grants-2012_12
ORD IDord-10c568ba34ec4f0c8e28401475fcefa8
Source noteuspto-grants-2012_12