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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436076Generated: October 30, 2026

Azobisisobutyronitrile → HCID 24784534, compound

https://huagongshe.com/reaction/1436076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-BromosuccinamideHCID 9834204—
ReactantHCID 24784533HCID 24784533—
SolventCarbon TetrachlorideHCID 5943—
SolventEthyl AcetateHCID 8857—
ProductHCID 24784534HCID 2478453454.1%

Reaction Steps

2-(4,4-Dimethyl-2-oxo-1,3-oxazolidin-3-yl)-4,5-dihydronaphtho[1,2-d][1,3]thiazole-7-carbonitrile (0.65 g, 2.0 mmol), prepared in step 5 of Example 6, N-bromosuccinamide (0.39 g, 2.2 mmol) and a catalytic amount of 2,2′-azobis(2-methylproprionitrile) were stirred in carbontetrachloride (68 mL) at reflux for 4 h. The reaction was diluted with ethyl acetate and washed with 10% sodium thiosulfate. The layers were separated and the organic layer was dried over anhydrous MgSO4, filtered and concentrated to give 0.64 g of crude product. Purification of the crude product on silica gel using a stepwise gradient of 6:1 to 1:1 hexane:ethyl acetate as the eluent gave 0.35 g of product that contained an impurity. Recrystallization from ethyl acetate afforded the title compound (0.02 g, 3%), mp>230° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618989B2
Source datasetuspto-grants-2009_11
ORD IDord-b10525d77d994e0d9d2c08d5103cd55e
Source noteuspto-grants-2009_11