참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Epichlorohydrin | HCID 7835 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Isostearyl Alcohol EX | HCID 62825 | — |
| 촉매 | Stearyltrimethylammonium chloride | HCID 8155 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | Isostearyl glycidyl ether | HCID 22622804 | 83.2% |
반응 단계
Into a round bottom flask having a capacity of 1 liter and equipped with a reflux condenser, a thermometer, a dropping funnel, and a stirring means, 120 g of a 50% sodium hydroxide solution (60 g (1.5 mole) as pure sodium hydroxide), 68 g (0.25 mole) of isostearyl alcohol [5,7,7-trimethyl-2-(1,3,3-trimethylbutyl) octanol], 200 ml of n-hexane, and 2.51 g (0.0075 mole) of stearyl trimethyl ammonium chloride, were introduced in this order. The reaction mixture was kept at a reaction temperature of 25° C. in a water bath, and while vigorously stirring the mixture at a stirring speed of 400 r.p.m., 93 g (1 mole) of epichlorohydrin was added dropwise from the dropping funnel. It took about 1.5 hours for the addition of the epichlorohydrin, and the reaction mixture was heated to 50° C. and stirred for about 8 hours at this temperature. After the completion of the reaction, the mixture was treated in a usual manner, whereupon 67.9 g (yield: 83%) of isostearyl glycidyl ether (5,7,7-trimethyl-2-(1,3,3-trimethylbutyl)-octyl glycidyl ether) was obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04465869 |
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| 출처 데이터셋 | uspto-grants-1984_08 |
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| ORD ID | ord-f627163b3e1b4da8aeca592dd6510e85 |
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| 출처 메모 | uspto-grants-1984_08 |
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