HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335431Generated: October 31, 2026
Tetrahydrofuran → 2-(1,3,5-Triethylphenyl)-2-oxoacetic acid
https://huagongshe.com/reaction/335431
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-(1,3,5-triethylphenyl)-2-oxoacetate | HCID 66691385 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(1,3,5-Triethylphenyl)-2-oxoacetic acid | HCID 66691561 | 92.1% |
Reaction Steps
To a 3 L volume four-necked flask, tetrahydrofuran (750 ml) and ethyl 2-(1,3,5-triethylphenyl)-2-oxoacetate (9-b) (261.0 g) were added, and sodium hydroxide (88 g) dissolved in water (237 g) was added dropwise thereto at about 15-20° C. The resulting mixture was stirred at room temperature for 1 hour and 30 minutes. The solid was removed by decantation. The liquid part was concentrated under reduced pressure. The residue was extracted with toluene and water. After the organic layer was removed, the aqueous layer was washed with toluene. The pH of the aqueous layer was adjusted to 1 with dilute sulfuric acid under cooling, and then the aqueous layer was extracted with toluene. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and filtered to remove the insolubles. The filtrate was concentrated under reduced pressure to give 214.8 g of 2-(1,3,5-triethylphenyl)-2-oxoacetic acid (8-b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08884010B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-40c898047fe544bc8034f86ce7bf96dd |
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| Source note | uspto-grants-2014_11 |
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