HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367768Generated: October 31, 2026
Benzyl Bromide → Benzene, [[(12-bromododecyl)oxy]methyl]-
https://huagongshe.com/reaction/1367768
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 12-Bromo-1-dodecanol | HCID 137895 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzene, [[(12-bromododecyl)oxy]methyl]- | HCID 11100339 | 73% |
Reaction Steps
12-Bromododecan-1-ol (1.83 g) was dissolved in 7 ml of dried THF, and sodium hydride (331.2 mg) was added to this solution. The reaction mixture was stirred at room temperature for 30 minutes, then benzyl bromide (0.99 ml) was added using a syringe, and the reaction mixture was refluxed for 24 hours while stirring. Saturated ammonium chloride solution was added to the reaction mixture, which was then extracted with diethyl ether. The organic layer was washed with saline solution, dried over magnesium sulfate, and filtered, and the solvent was distilled off under reduced pressure. Purification of the residue by silica gel flash chromatography (hexane:dichloromethane=8:2) gave 1-((12-bromododecanoxy)methyl)benzene as a colorless oil at a 73% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893304B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-d7bb9c06732b431d94ea8e06249d7b81 |
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| Source note | uspto-grants-2011_02 |
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