HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573028Generated: October 25, 2026
Hydrochloric Acid → 2,7-Didocosyloxy-9-fluorenone
https://huagongshe.com/reaction/573028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromodocosane | HCID 81355 | — |
| Reactant | 2,7-Dihydroxyfluoren-9-one | HCID 4354181 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,7-Didocosyloxy-9-fluorenone | HCID 66719095 | 107.5% |
Reaction Steps
2,7-Dihydroxy-9-fluorenone (1 g, 4.71 mmol) was dissolved in DMF (40 ml), and potassium carbonate (1.95 g, 14.1 mmol) and docosyl bromide (96%, 4.02 g, 9.91 mmol) were added. The mixture was stirred overnight at 80° C., docosyl bromide (0.40 g, 0.99 mmol) was further added and the mixture was stirred overnight. After completion of the reaction, the reaction mixture was cooled to room temperature, 1N hydrochloric acid (120 ml) was added thereto in a water bath to allow precipitation. The crystals were collected by filtration and slurry washed once with 1N hydrochloric acid (40 ml), once with pure water (40 ml) and once with methanol (40 ml) to give 2,7-didocosyloxy-9-fluorenone (4.20 g, docosyl bromide mixture).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029504B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-4b2220a64d72410ba99bbe69369cf75f |
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| Source note | uspto-grants-2015_05 |
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