참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 1,3-Dibromopropane | HCID 8001 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 2,2-Dimethyl-4-pentenoic acid | HCID 140065 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1,3-Bis(2,2-dimethyl-4-pentenoyloxy)-propane | HCID 19745526 | 68.5% |
반응 단계
To a mixture of 2.6 g (0.02 mole) of 2,2-dimethyl-4-pentenoic acid (XII) and 50 ml of hexamethylphosporic triamide a solution of 1.2 g (0.03 mole) of sodium hydroxide in 3.6 ml of water is added. The reaction mixture is stirred at room temperature for 1 hour and then 1.2 ml (2.4 g, 0.012 mole) of 1,3-dibromopropane are added. The mixture is stirred at room temperature for 4 hours, then poured onto 100 ml of 5% aqueous hydrochloric acid and extracted twice with 50 ml of diethyl ether each. The organic phase is washed twice with 25 ml of water each, dried over sodium sulfate and the solvent is distilled off under reduced pressure. The crude product thus obtained is purified by chromatography on a silica gel column eluted with a 7:3 mixture of hexane and diethyl ether. Thus 2.03 g of the desired compound are obtained in the form of a colourless oil. Yield: 68.5%. According to TLC chromatography using the above-specified eluent Rf =0.6.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05155260 |
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| 출처 데이터셋 | uspto-grants-1992_10 |
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| ORD ID | ord-d0e06574e7ca4cc7951fc21f74d5cc03 |
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| 출처 메모 | uspto-grants-1992_10 |
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