참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethylene Glycol | HCID 174 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 4-tert-Butyl-3-hydroxy-2,6-xylylacetonitrile | HCID 108756 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-(4-tert-Butyl-3-hydroxy-2,6-dimethylphenyl)acetic acid | HCID 20345905 | — |
반응 단계
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 homogenous at about 116° to 117° and was heated at this temperature for 2 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°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04075161 |
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| 출처 데이터셋 | uspto-grants-1978_02 |
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| ORD ID | ord-a87ac562427a47849c689a446715abb0 |
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| 출처 메모 | uspto-grants-1978_02 |
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