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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415693Generated: October 28, 2026

Azobisisobutyronitrile → 2-Bromomethyl-6-phenoxy-benzothiazole

https://huagongshe.com/reaction/415693

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 numberUS08088791B2
Source datasetuspto-grants-2012_01
ORD IDord-b63ce5b79cff4ef494c7a7f06aa72691
Source noteuspto-grants-2012_01