HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909118Generated: October 26, 2026
Water → 3-(3,7-Dimethyloctyloxy)bromobenzene
https://huagongshe.com/reaction/909118
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 3-Bromophenol | HCID 11563 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Bromo-3,7-dimethyloctane | HCID 137914 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(3,7-Dimethyloctyloxy)bromobenzene | HCID 18004181 | 92% |
Reaction Steps
Under an inert atmosphere, 90 g of 3-bromophenol was dissolved in 600 ml of ethanol. Further, 39 g potassium hydroxide was added to this and the mixture was heated up to 70° C. for dissolution thereof. From a dropping funnel, 126 g of 3,7-dimethylbromooctane was dropped over 15 minutes. After completion of dropping, the mixture was heated to 84° C. and stirred for about 22 hours under heat. After completion of heating, the mixture was left to cool to room temperature. The reaction solution was bisected, 500 ml of water was added to respective portions, then, ethanol was distilled off by an evaporator. The solutions after distilling off of ethanol were combined and trisected, 300 ml of ethyl acetate was added to respective portions to cause liquid separation, and the organic layers were washed with 200 ml of water twice. The organic layers were combined and the solvent was distilled off by an evaporator, then, the residue was dried by heating at 90° C. for 5 hours under vacuum by a rotary pump. About 150 g of 3-(3,7-dimethyloctyloxy)-bromobenzene was obtained as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017721B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-47f7d629a9fe45f69ea8c7869ad0ada3 |
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| Source note | uspto-grants-2011_09 |
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