HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573029Generated: October 31, 2026
Hydrochloric Acid → HCID 86645784, compound
https://huagongshe.com/reaction/573029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Behenyl Alcohol | HCID 12620 | — |
| Reactant | 1,12-Dibromododecane | HCID 18766 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86645784 | HCID 86645784 | 78% |
Reaction Steps
Sodium hydride (60%, 0.98 g, 24.5 mmol) washed with hexane was suspended in toluene (16 ml), 1-docosanol (4.00 g, 12.2 mmol) was added, 1,12-dibromododecane (8.04 g, 24.5 mmol) was added, and the mixture was stirred at 85° C. for 2 days. The reaction mixture was cooled to room temperature, 1N hydrochloric acid (30 ml) was added dropwise thereto in a water bath to quench the reaction. The mixture was extracted with chloroform (100 ml), and washed 3 times with 1N hydrochloric acid (30 ml), 3 times with 5% aqueous sodium hydrogen carbonate solution (30 ml), and once with 20% aqueous sodium chloride solution (30 ml). The organic layer was dried over sodium sulfate, and the solvent of the filtrate was evaporated. The residue was isolated and purified by silica gel column chromatography and precipitated with methanol (70 ml) to give 12-docosyloxy-dodecyl bromide (yield 78%).
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-dc0a9c05ed624003a7bdaffa1a49d96c |
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| Source note | uspto-grants-2015_05 |
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