참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | 7-(2-Tetrahydropyranyloxy)heptanenitrile | HCID 20542932 | — |
| 반응물 | Diisobutylaluminumhydride | HCID 21225700 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 7-(Oxan-2-yloxy)heptanal | HCID 182184 | — |
반응 단계
Diisobutylaluminium hydride (19.4 g.) in dry benzene (50 ml.) was added dropwise at 10° C. to a stirred solution of 7-(2-tetrahydropyranyloxy)heptanenitrile (20.6 g.) in dry diethyl ether (200 ml.). The solution was stirred at 10° C. for 30 minutes and was then added to 2 N aqueous sulphuric acid (300 ml.) at 0° C. The mixture was heated at 30° C. for 30 minutes, and then saturated with sodium chloride and the layers were separated. The aqueous layer was extracted with diethyl ether and the combined organic layers were washed with aqueous sodium bicarbonate, and then aqueous sodium chloride, and dried over sodium sulphate. The solvent was evaporated and the residue was distilled under reduced pressure to give 7-(2-tetrahydropyranyloxy)-heptanal (12.7 g.), b.p. 78°-106° C./0.1 mm.Hg, nD25 1.456.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04036872 |
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| 출처 데이터셋 | uspto-grants-1977_07 |
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| ORD ID | ord-e0f7acbedf3840f39f01f385dd8e247c |
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| 출처 메모 | uspto-grants-1977_07 |
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