참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | Methyl valerate | HCID 12206 | — |
| 반응물 | 1-Pentene, 5-bromo- | HCID 70704 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 용매 | Butyllithium | HCID 178418339 | — |
| 생성물 | Methyl 2-propyl-6-heptenoate | HCID 20462871 | 43.2% |
반응 단계
To a solution of lithium diisopropyl amide, which was prepared from diisopropylamine (6.6 g) in dry tetrahydrofuran (50 ml) and 15% butyl lithium in hexane solution (38 ml) at -65° to -60° C. in a nitrogen atmosphere, were added dropwise a solution of methyl pentanoate (7 g) in dry tetrahydrofuran (65 ml) followed by a solution of 5-bromo-1-pentene (9 g) in dry tetrahydrofuran (30 ml) at the same temperature. The mixture was stirred for 4 hours at -65° to 0° C. All the operations described above were carried out in a nitrogen atmosphere. Diluted hydrochloric acid (25 ml) and toluene (200 ml) were added at 0° C. to the mixture, which was further stirred. The organic layer was separated, washed with water, dried and concentrated. The resulting oily residue (9 g) was purified by silica gel column chromatography to give colorless oil of methyl 2-propyl-6-heptenoate (4.8 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04443365 |
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| 출처 데이터셋 | uspto-grants-1984_04 |
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| ORD ID | ord-03a8983bed7549a7883f36fce2efdad2 |
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| 출처 메모 | uspto-grants-1984_04 |
|---|