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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538619Generated: October 31, 2026

Azobisisobutyronitrile → 2-Bromomethyl-6-phenoxy-benzothiazole

https://huagongshe.com/reaction/538619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methyl-6-phenoxy-benzothiazoleHCID 3838252—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromomethyl-6-phenoxy-benzothiazoleHCID 594030457.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-methyl-6-phenoxy-benzothiazole (0.06 g, 0.24 mmol) in 5 ml of CCl4 was added NBS (0.039 g, 0.22 mmol) and AIBN (0.004 g, 0.024 mmol). The reaction mixture was heated at 100° C. for 2 h under nitrogen atmosphere. After the completion of the reaction mixture (TLC monitoring), the reaction mixture was evaporated to dryness under reduced pressure and the residue was purified by column chromatography on silica (230-400M) using 1% ethyl acetate/hexane eluent to give the desired product (0.005 g, 6.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865736B2
Source datasetuspto-grants-2014_10
ORD IDord-015d57a6684143aa814cf189b3eb25ce
Source noteuspto-grants-2014_10