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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356099Generated: October 25, 2026

Azobisisobutyronitrile → 2,6-Dichloro-3-nitrobenzyl Bromide

https://huagongshe.com/reaction/356099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantEthyl AcetateHCID 8857—
Reactant2,6-Dichloro-3-nitrotolueneHCID 97155—
ReactantDibromohydantoinHCID 54068228—
SolventChlorobenzeneHCID 7964—
Product2,6-Dichloro-3-nitrobenzyl BromideHCID 11011535—

Reaction Steps

A mixture of dibromohydantoin (70 g, 0.24 mol) and AIBN (5 g) was added in portions, at 150° C., to 2,6-dichloro-3-nitrotoluene (100 g, 0.48 mol) in chlorobenzene (400 ml). A mixture of dibromohydantoin (35 g, 0.12 mol) and AIBN (2.5 g) was added once again after 1 h. After a further 1.5 h, the mixture was allowed to cool down and ethyl acetate (500 ml) was added. This mixture was washed once, in each case, with saturated Na2SO3, Na2CO3 and NaCl solution, dried (MgSO4) and concentrated, when the title compound resulted as an amorphous powder. ##EQU1## b) 4-(2,6-Dichloro-3-nitrobenzyloxy)benzothiazole

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834500
Source datasetuspto-grants-1998_11
ORD IDord-c67fcee6818b44f9bd1756eb14aa2056
Source noteuspto-grants-1998_11