참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Myristyl bromide | HCID 8208 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 2,3-Bis(hexadecyloxy)propan-1-ol | HCID 102548 | — |
| 반응물 | Benzylglycerol | HCID 2735483 | — |
| 반응물 | 1-Hexadecyl-2-tetradecyl-3-trityl glycerol | HCID 57129051 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3-(Hexadecyloxy)-2-(tetradecyloxy)propan-1-OL | HCID 57128111 | — |
반응 단계
1-hexadecyl glycerol (105 g, 0.33 mol) and 93 g (0.33 mol) tritylchloride were dissolved in 300 ml of pyridine. The mixture was heated at 100° C. for 16 hours. After cooling to room temperature 1500 ml of ethyl ether was added and the slurry washed 3 times with cold 0.5N H2SO4, 5% sodium bicarbonate and 2 times with water. The organic phase was dried over MgSO4, the ether removed on a rotary evaporator and the residue recrystallized from ethanol, yielding the intermediate 1-hexadecyl-3-trityl glycerol (129 g, 70%). The 2 position of this intermediate was alkylated with tetradecyl bromide in the same manner (powdered KOH in toluene) as described earlier for the dialkylation of benzyl glycerol in the preparation of 1,2-dihexadecyl glycerol. The resulting 1-hexadecyl-2-tetradecyl-3-trityl glycerol (128g) was dissolved in 300 ml of petroleum ether. At room temperature 30g of anhydrous hydrogen chloride was added. A precipitate formed within a short time. The slurry was stirred at room temperature for 4 hours and then filtered. The solids were recrystallized from acetone (10° C.) to give 45.6g of product, m.p. 42°-3° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05439669 |
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| 출처 데이터셋 | uspto-grants-1995_08 |
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| ORD ID | ord-da3bd6221bbd4f568006381924c4c0bf |
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| 출처 메모 | uspto-grants-1995_08 |
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