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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 903298생성일: 2026년 10월 27일

Propyne → beta-Damascenone, (2Z)-

https://huagongshe.com/reaction/903298

반응식

참여 물질

역할이름HCID투입량
반응물PropyneHCID 6335—
반응물3,7-Dimethylocta-2,6-DienalHCID 8843—
반응물2,6,6-Trimethyl-1-[1-hydroxy-2-butynyl]-1,3-cyclohexadieneHCID 23338079—
반응물6,10-Dimethylundeca-2,5,9-trien-4-oneHCID 54158364—
반응물6,10-Dimethyl-4-hydroxy-2,5,9-undecatrieneHCID 54549445—
반응물2,6,6-Trimethyl-1-tetrolyl-1,3-cyclohexadieneHCID 70587951—
촉매Manganese dioxideHCID 14801—
생성물beta-Damascenone, (2Z)-HCID 12309006—

반응 단계

Safranal, prepared according to Compt. rend. 262, 1725 (1966), was reacted with propyne to give 2,6,6-trimethyl-1[-1-hydroxy-2-butynyl]-1,3-cyclohexadiene, following the procedure outlined in Example 18, paragraph (b), for the reaction of citral with propyne. The above carbinol was oxidised with MnO2 to 2,6,6-trimethyl-1-tetrolyl-1,3-cyclohexadiene, following the procedure described in Example 18, paragraph (c), for the oxidation of the dihydro analogue. The above acetylenic ketone was then partially reduced to the title compound following the method described in Example 18, paragraph (a). Cis-2,6,6-trimethyl-1-crotonoyl-1,3-cyclohexadiene gave the following NMR data (CCl4): 1.06 (6 H, s), 1.69 (3 H, s), 2.09 (2 H, d, J=2.3 cps), 2.14 (3 H, d, J=5.5 cps), 5.81 (2 H, t+s, J=2.3 cps), 6.2 (2 H, complex band) ppm (δ).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04226892
출처 데이터셋uspto-grants-1980_10
ORD IDord-f66eca6e31c14bd4a34efc6fe40fc400
출처 메모uspto-grants-1980_10