참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Propargyl bromide | HCID 7842 | — |
| 반응물 | 1,1-Dibromoethane | HCID 11201 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 2-Pentanone, 5-chloro- | HCID 79993 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 7-Chloro-4-hydroxy-4-methyl-1-heptyne | HCID 12898739 | — |
반응 단계
To a mixture of 6.69 g. of magnesium in 20 ml. of ether under argon, is added 0.1 g. of mercuric chloride and 0.1 g. of dibromoethane. The mixture is stirred for 10 minutes and 0.5 ml. of propargyl bromide is added. A 50 ml. portion of ether is added, followed by a solution of 30 g. of 5-chloro-2-pentanone and 32.55 g. of propargyl bromide in 45 ml. of ether with stirring, at a rate to maintain vigorous reflux. The mixture is stirred an additional 15 minutes, cooled to -5° C. and an ice cold saturated solution of ammonium chloride is added dropwise. The ether layer is decanted and filtered. The solids are washed with ether which is also filtered. The combined ether filtrates are washed with water, dried over magnesium sulfate and the solvent removed giving the product as an orange oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04254036 |
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| 출처 데이터셋 | uspto-grants-1981_03 |
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| ORD ID | ord-6df25f8fcda442fa8959ab015a89da1c |
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| 출처 메모 | uspto-grants-1981_03 |
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