참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl Methacrylate | HCID 6658 | — |
| 반응물 | 4-Methoxyphenol | HCID 9015 | — |
| 반응물 | 1-(Piperidin-1-yl)ethanol | HCID 3030541 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 2-(1-Piperidinyl)ethyl 2-methyl-2-propenoate | HCID 580183 | — |
반응 단계
A 1 liter resin kettle was fitted with an air bubbler, temperature probe and still head. To the kettle was added, in order: 233 grams piperidinoethanol, 5.0 grams sodium methoxide, 0.5 grams p-methoxy phenol (to inhibit polymerization), and 750 milliliters methyl methacrylate. With a slow stream of air bubbling through the reaction mixture, the mixture was stirred vigorously and heated to 80 degrees with a constant temperature water bath. 5.0 grams sodium methoxide were added 30 and 60 minutes after the start of the reaction. After 120 minutes, the reaction mixture was cooled and neutralized with 17.0 grams acetic acid. The reaction mixture was transferred to a separatory funnel. The product was extracted from the reaction mixture into one liter of aqueous solution containing 95 grams concentrated sulfuric acid. The reaction mixture was treated with 500 milliliters of aqueous solution containing 15 grams concentrated sulfuric acid to extract remaining product. The two aqueous portions were combined and extracted with petroleum ether (boiling point 30-60 degrees) to remove residual methyl methacrylate, then rendered basic with 500 milliliters of aqueous solution containing 150 grams potassium hydroxide. The product was extracted from the aqueous solution with petroleum ether. The petroleum ether solution was dried over anhydrous magnesium sulfate. The petroleum ether was removed from the product with a rotary film evaporator under reduced pressure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04735887 |
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| 출처 데이터셋 | uspto-grants-1988_04 |
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| ORD ID | ord-16fb39f0d69a4064853fe35cce48be2e |
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| 출처 메모 | uspto-grants-1988_04 |
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