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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472770Generated: October 31, 2026

Sodium Azide → HCID 178426092, compound

https://huagongshe.com/reaction/1472770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant4,5-Bis(4-chloro-2-methylphenyl)thiophene-2-carbonitrileHCID 68293634—
CatalystZinc bromideHCID 10421208—
ProductHCID 178426092HCID 17842609290%

Reaction Conditions

Temperature110 °C

Reaction Steps

A round-bottomed flask was charged with 4,5-bis(4-chloro-2-methylphenyl)thiophene-2-carbonitrile (600 mg, 1.67 mmol), zinc bromide (945 mg, 4.20 mmol) and sodium azide (273 mg, 4.20 mmol). After degassed, DMF (5 mL) was added. The reaction mixture was heated to 110° C. and stirred at this temperature until complete. The reaction was cooled to rt, and 30 mL of 0.1 N aqueous HCl was added. The reaction mixture was extracted with ethyl acetate. The organic phase was dried over anhydrous sodium sulphate and then concentrated. The residue was purified by flash chromatography (hexane:EtOAc:AcOH=30:10:1). 603 mg (90%) of product was obtained as a white solid, 1H NMR (DMSO, 500 MHz) δ 7.82 (s, 1H), 7.36 (d, J=2.04 Hz, 1H), 7.34 (d, J=1.94 Hz, 1H), 7.31 (d, J=8.25 Hz, 1H), 7.28 (dd, J1=8.26 Hz, J2=1.99 Hz, 1H), 7.17 (dd, J1=8.20 Hz, J2=2.05 Hz, 1H), 7.02 (d, J=8.28 Hz, 1H), 2.17 (s, 3H), 2.03 (s, 3H); 13C NMR (DMSO, 125 MHz) δ 140.58, 139.14, 139.12, 138.19, 133.59, 133.39, 132.94, 132.47, 131.71, 131.17, 130.57, 130.17, 130.11, 126.00, 125.80, 19.69, 19.57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012655B2
Source datasetuspto-grants-2015_04
ORD IDord-b70980c576cb4e259c4189f46ddbfd8d
Source noteuspto-grants-2015_04