Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472788Generated: October 31, 2026

Sodium Azide → HCID 178422382, compound

https://huagongshe.com/reaction/1472788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantHCID 68293613HCID 68293613—
CatalystZinc bromideHCID 10421208—
ProductHCID 178422382HCID 17842238291%

Reaction Conditions

Temperature130 °C

Reaction Steps

A round-bottomed flask was charged with 4,5-bis(4-chloro-2-isopropylphenyl)-3-methylthiophene-2-carbonitrile (190.5 mg, 0.44 mmol), zinc bromide (338 mg, 1.50 mmol) and sodium azide (97.5 mg, 1.50 mmol). After degassed, DMF (3 mL) was added. The reaction mixture was heated to 130° 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). 188.7 mg (90%) of product was obtained as a white solid, 1H NMR (CDCl3, 500 MHz) δ 7.25-7.22 (m, 2H), 7.18 (dd, J1=8.18 Hz, J2=2.13 Hz, 1H), 7.09-7.06 (m, 2H), 7.02 (d, J=8.20 Hz, 1H), 3.04 (sep, J=6.75 Hz, 1H), 2.74 (sep, J=6.80 Hz, 1H), 2.37 (s, 3H), 1.12 (d, J=6.80 Hz, 3H), 1.05 (d, J=6.80 Hz, 6H), 0.90 (d, J=6.80 Hz, 3H); 13C NMR (CDCl3, 125 MHz) δ 150.32, 149.87, 141.11, 140.81, 140.72, 135.33, 134.47, 132.72, 132.02, 131.51, 129.01, 126.30, 126.20, 125.84, 125.52, 30.35, 30.10, 24.76, 23.60, 23.13, 15.78.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012655B2
Source datasetuspto-grants-2015_04
ORD IDord-e473018213de4f9e9a4e092fb0863e65
Source noteuspto-grants-2015_04