HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243268Generated: November 2, 2026
Boron tribromide → 2-(4-Hydroxyphenyl)-6-(4-nonylphenyl)benzothiazole
https://huagongshe.com/reaction/1243268
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-(4-Dodecyloxyphenyl)-6-(4-nonylphenyl)benzothiazole | HCID 21924524 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Hydroxyphenyl)-6-(4-nonylphenyl)benzothiazole | HCID 135761779 | 77.4% |
Reaction Steps
Boron tribromide (0.53 cm3, 5.65×10−3 mol) was added dropwise to a cooled (0° C.) stirred solution of 2-(4-dodecyloxyphenyl)-6-(4-nonylphenyl)benzothiazole (2.25 g, 3.76×10−3 mol) in dichloromethane (100 cm3). The reaction mixture was stirred at room temperature overnight, then poured onto an ice/water mixture (200 g) and stirred (30 min). The reaction mixture was extracted with dichloromethane (2×75 cm3) and the combined organic layers were washed with brine (2×100 cm3) and dried (MgSO4). After filtration the solvent was removed under reduced pressure and the residue was purified by column chromatography [silica gel, ethyl acetate:hexane 1:1] followed by recrystallisation from ethyl acetate to yield 1.25 g (77.3%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07118787B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-33520a08346448e58f6074d2f382d4e6 |
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| Source note | uspto-grants-2006_10 |
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