HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049133Generated: November 1, 2026
Ethylene Glycol → 2-(4-tert-Butyl-3-hydroxy-2,6-dimethylphenyl)acetic acid
https://huagongshe.com/reaction/2049133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-tert-Butyl-3-hydroxy-2,6-xylylacetonitrile | HCID 108756 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-tert-Butyl-3-hydroxy-2,6-dimethylphenyl)acetic acid | HCID 20345905 | — |
Reaction Steps
65.1 grams of the compound of Example 3 was added with stirring to a solution of 36 grams of sodium hydroxide in 40 ml of ethylene glycol and 66 ml of water. The reaction mixture became homogeneous at about 116° to 117° and was heated at this temperature for two hours. The reaction mixture was cooled by the addition of chopped ice and cold water to the reaction mixture to make a total volume of one liter. After clarifying the reaction mixture by filtration, the filtrate was made acid with concentrated aqueous hydrochloric acid, yielding a white precipitate, which was filtered, washed with cold water and dried. The product was then treated with rapid stirring at 50° C. with about 800 ml of 6% sodium bicarbonate solution until carbon dioxide evolution stopped. The turbid solution was filtered free of a white solid by-product. (A). The clarified filtrate was made acid with concentrated hydrochloric acid while cooling, and the resulting white precipitate filtered. After washing with hot water and drying the product was obtained as a white powder melting at 161° to 165°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04196301 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-f4de1727579e458ebc62ecb7ba50846d |
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| Source note | uspto-grants-1980_04 |
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