HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643181Generated: October 29, 2026
1-Bromododecane → 2,5-Dibromo-4-(dodecyloxy)phenol
https://huagongshe.com/reaction/643181
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromododecane | HCID 8919 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,5-Dibromohydroquinone | HCID 280945 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,5-Dibromo-4-(dodecyloxy)phenol | HCID 66760725 | 60% |
Reaction Steps
2,5-Dibromohydroquinone 3 (40.2 g, 0.15 mol) was dissolved in a solution of sodium hydroxide (9.2 g, 0.23 mol) in 1.5 L of absolute ethanol at room temperature under nitrogen atmosphere. The reaction mixture was warmed to 50-60° C. with constant stirring. The dodecylbromide (36 ml, 0.15 mol) was added drop wise to the above reaction mixture at 60° C. After 10 h of stirring under nitrogen atmosphere, the reaction mixture was cooled and the precipitate formed was filtered and washed with methanol. This precipitate was identified as dialleylated-2,5-dibromohydroquinone as a side product. The filtrate was evaporated to remove the solvent. 2 L of distilled water was added to the residue and the mixture was acidified with 36% HCl, boiled gently for 1 h and cooled. The resulting precipitate was collected by filtration, washed with water and dried in vacuo. The crude product was purified by column chromatography using a mixture of solvents (CH2Cl2: hexanes, 4:6) to get the pure product in 60% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700040B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-696af86c369949ada4c717ca3814bfb5 |
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| Source note | uspto-grants-2010_04 |
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