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HRID 1074645생성일: 2026년 10월 26일

Acetic Acid → 3-Oxo-alpha-ionone

https://huagongshe.com/reaction/1074645

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Ammonium BromideHCID 25514—
반응물Alpha-IononeHCID 5282108—
촉매Cobalt(II) acetate tetrahydrateHCID 61372—
용매CyclohexaneHCID 8078—
생성물3-Oxo-alpha-iononeHCID 5363685—

반응 단계

Items 1-6 given in Table 1 hereinafter are carried out following the procedure of Example 1 substituting therein 5 g of 92% α-ionone for the 40 g of 98% α-ionone, 1.3 g (20 mol percent) of cobalt acetate tetrahydrate for the 10.4 g, and 0.7 g, (27 mol percent) of ammonium bromide for the 4.0 g. The amount of solvent substituting for glacial acetic acid and cyclohexane is represented in Table 1 and amounts to 60 ml. The yields of 3,5,5-trimethyl-4-[(E)-3-oxo-1-butenyl]-2-cyclohexen-1-one (3-oxo-α-ionone) are determined by gas chromatography (GC). It will be observed that the sum of all products appearing in the gas chromatogram only amounts to a maximum of about 60% of the total weight. The remainder probably consists of oligomeric by-products. The oxidation conditions are not optimized.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04393243
출처 데이터셋uspto-grants-1983_07
ORD IDord-792a6b9d0d4b4b698db31596822e5214
출처 메모uspto-grants-1983_07