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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325813생성일: 2026년 10월 24일

Hydrochloric Acid → Methyl 2-propyl-6-heptenoate

https://huagongshe.com/ko/reaction/325813

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DiisopropylamineHCID 7912—
반응물Methyl valerateHCID 12206—
반응물1-Pentene, 5-bromo-HCID 70704—
반응물Lithium diisopropylamideHCID 2724682—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매ButyllithiumHCID 178418339—
생성물Methyl 2-propyl-6-heptenoateHCID 2046287143.2%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04443365
출처 데이터셋uspto-grants-1984_04
ORD IDord-03a8983bed7549a7883f36fce2efdad2
출처 메모uspto-grants-1984_04