HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460853Generated: October 30, 2026
4-tert-Butylphenol → HCID 22759343, compound
https://huagongshe.com/reaction/460853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 22759269 | HCID 22759269 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22759343 | HCID 22759343 | — |
Reaction Steps
A mixture of ethyl 8-acetyl-12,13-epoxytridecanoate (14.9 g., 0.05 mole), 4-tert-butylphenol (11.2 g., 0.075 mole), sodium hydroxide (7.0 g., 0.175 mole), water (30 ml.) and tetrahydrofuran (200 ml.) is stirred 4 hours at 40°-45°, 17 hours at 25° and one hour on the steam bath letting the tetrahydrofuran slowly boil away. The residue is treated with water and extracted with ether. The aqueous solution is acidified with hydrochloric acid. The oily product is taken up in ether. The ether is evaporated and the residue treated with a solution of 16.8 g. sodium bicarbonate in 275 ml. of water. The resulting solution is extracted twice with ether to remove the excess weakly acidic phenol. The aqueous solution is acidified, the product taken up in ether, washed with water and dried over sodium sulfate. The ether is evaporated leaving 10.2 g. of the crude title compound as a yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04061643 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-d9216d3589c44d7499a971325eb502a4 |
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| Source note | uspto-grants-1977_12 |
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