HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573965Generated: October 31, 2026
1-Bromooctadecane → 2,3,4-Trioctadecanoxybenzophenone
https://huagongshe.com/reaction/573965
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromooctadecane | HCID 8218 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Alizarin Yellow A | HCID 70837 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,3,4-Trioctadecanoxybenzophenone | HCID 59510351 | 91.3% |
Reaction Steps
Under an argon atmosphere, 2,3,4-trihydroxybenzophenone (1.61 g, 7.00 mmol), 1-bromooctadecane (7.32 g, 22.0 mmol) and potassium carbonate (4.35 g, 31.5 mmol) were added to dehydrating N,N-dimethylformamide (30 mL), and the mixture was stirred at 80° C. overnight. After completion of the reaction, purified water (200 mL) was added to the reaction mixture, the mixture was stirred for 1 hr, and the precipitated solid was collected by filtration. The obtained solid was slurry-washed in methanol and, after filtration, dried under reduced pressure to give the title compound (6.31 g, 91.1%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029528B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-9c3ace18d0934304bb2c6f9ad57f2525 |
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| Source note | uspto-grants-2015_05 |
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