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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 708934생성일: 2026년 10월 26일

5-Methyl-2-hepten-4-one (natural) → S-(5-methyl-4-oxoheptan-2-yl) ethanethioate

https://huagongshe.com/reaction/708934

반응식

참여 물질

역할이름HCID투입량
반응물5-Methyl-2-hepten-4-one (natural)HCID 517791—
반응물HCID 178418634HCID 178418634—
촉매PiperidineHCID 8082—
생성물S-(5-methyl-4-oxoheptan-2-yl) ethanethioateHCID 8672332890%

반응 조건

온도15 °C

반응 단계

A reaction flask was charged with 5-methyl-2-hepten-4-one (200 g, 1.59 mol) and piperidine (6.6 g), and cooled to 15° C. using a cooling bath. Thioacetic acid (241 g, 3.17 mol) was subsequently added to the reaction flask dropwise through an addition funnel The feeding was exothermic. The reaction temperature was kept below 25° C. After the addition was completed, the cooling bath was removed while the reaction was stirred for another hour at room temperature. The reaction mixture was then transferred into a separatory funnel. The organic layer was washed with sodium bicarbonate solution (10%, 250 mL) followed by brine (250 mL), and dried with magnesium sulfate. Further distillation of the obtained crude product under a vacuum (at 78° C. with a pressure of 11.0 mmHg) provided S-(5-methyl-4-oxoheptan-2-yl) ethanethioate (288.0 g) (about 90% yield with a purity over 97% monitored with gas chromatography).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09179701B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-a5e004f3da4b40b7a4e7c220e8fcf4f9
출처 메모uspto-grants-2015_11