HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650808Generated: October 31, 2026
1-Bromododecane → Benzeneacetic acid, 4-(dodecyloxy)-
https://huagongshe.com/reaction/1650808
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromododecane | HCID 8919 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-hydroxyphenylacetate | HCID 28310 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzeneacetic acid, 4-(dodecyloxy)- | HCID 10336152 | 63% |
Reaction Steps
To a dimethylformamide (DMF, 100 ml) solution of ethyl 4-hydroxyphenylacetate (18 g, 0.1 mol.) and dodecyl bromide (25 g, 0.1 mol.) was added potassium carbonate (15 g, 0.1 mol.). The mixture was stirred at 100° C. for one hour. To the reaction solution, after cooling, was added water (200 ml) and the mixture was subjected to extraction with isopropyl ether (IPE). The organic layer was washed with water, dried and concentrated under reduced pressure. The concentrate was dissolved in a mixture of methanol (100 ml) and tetrahydrofuran (THF, 100 ml). To the solution was added aqueous sodium hydroxide (10 g, 0.25 mol.), and the mixture was stirred at 50° C. The reaction solution was concentrated under reduced pressure, whose pH was adjusted to 4, followed by extraction with ethyl acetate. The organic layer was washed with water, dried and concentrated under reduced pressure to leave crude crystals. Recrystallization from hexane-IPE gave 4-dodecyloxyphenylacetic acid (1-e, 20 g, 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04925868 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-16aebde31c074e54a8d11bff05acfb7c |
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| Source note | uspto-grants-1990_05 |
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