HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620706Generated: October 29, 2026
1-Bromooctane → 1-(Octyloxy)-4-(2,4,4-trimethylpentan-2-yl)benzene
https://huagongshe.com/reaction/620706
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | 4-Tert-octylphenol | HCID 8814 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Octyloxy)-4-(2,4,4-trimethylpentan-2-yl)benzene | HCID 21244005 | 81% |
Reaction Steps
To 700 ml of N,N-dimethylformamide were added 206 g of 4-t-octylphenol and 207 g of anhydrous potassium carbonate and the mixture was stirred at 50° C. To the mixture was added dropwise 251 g of 1-bromooctane and thereafter the mixture was stirred for 7 hours at 65° to 80° C. Then, after removing insoluble matter by filtration, water was added to the filtrate thus obtained and the product was extracted with ethyl acetate. The organic solvent layer was collected, washed with a saturated aqueous sodium chloride solution, dried on anhydrous magnesium sulfate, and concentrated under reduced pressure. The oily material thus obtained was distilled under reduced pressure (169°-172° C./0.05-0.06 mmHg) to provide 257 g (81% in yield) of 1-octyloxy-4-t-octylbenzene (Compound A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04822730 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-b3baf37056c242aab44d43951e06d2e4 |
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| Source note | uspto-grants-1989_04 |
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