HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415693Generated: October 28, 2026
Azobisisobutyronitrile → 2-Bromomethyl-6-phenoxy-benzothiazole
https://huagongshe.com/reaction/415693
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methyl-6-phenoxy-benzothiazole | HCID 3838252 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Bromomethyl-6-phenoxy-benzothiazole | HCID 59403045 | 7.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088791B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-b63ce5b79cff4ef494c7a7f06aa72691 |
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| Source note | uspto-grants-2012_01 |
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