참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,7-Dimethylocta-2,6-Dienal | HCID 8843 | — |
| 반응물 | 1-Bromo-1-propene | HCID 11533 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6,10-Dimethyl-4-hydroxy-2,5,9-undecatriene | HCID 54549445 | — |
반응 단계
12 g. of magnesium turnings were suspended under nitrogen in 250 ml. of dry tetrahydrofuran. Between 60° and 65°, 60 g. of 1-bromopropene dissolved in 50 ml. of tetrahydrofuran were added dropwise. During the addition, to prevent escaping of 1-bromopropene, the reflux condenser fitted on the reaction flask was cooled to -40°/-50°. When all Mg had reacted, the mixture was cooled to 20° and 76 g. of citral was added dropwise with cooling. After standing overnight, the mixture was poured into 1.5 liter of concentrated aqueous NH4Cl at 0°. The mixture was extracted 3 times with ether and the combined ether extracts treated as usual. After distillation, 6,10-dimethyl-4-hydroxy-2,5,9-undecatriene, b.p. 70°/0.1 Torr was obtained as a liquid with following constants: nD20 = 1.4950; d420 = 0.9145.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US03931326 |
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| 출처 데이터셋 | uspto-grants-1976_01 |
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| ORD ID | ord-eaad6f60373641808059047a6d426abb |
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| 출처 메모 | uspto-grants-1976_01 |
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