Ethylbenzene → 4-Hydroxypentan-2-one

HRID 925010ノート

反応式

HRID 925010 の反応式
C=CC1C=CC=CC=1.C1(C#C)C=CC=CC=1.C(C1C=CC=CC=1)C.C1CCCCC=1.C=CCCCC.[C:37]([CH2:40][C:41](=[O:43])[CH3:42])(=[O:39])[CH3:38]>C(O)(C)C.CC(C)=O>[CH3:42]/[C:41](/[O-:43])=[CH:40]/[C:37]([CH3:38])=[O:39].[OH:43][CH:41]([CH3:42])[CH2:40][C:37](=[O:39])[CH3:38]

参加物

10

実験手順

To study the scope of the catalytic activity of the SiO2@Pd-PAMAM microspheres, the catalytic hydrogenation reactions of substrates other than styrene were explored (Table 3). For instance, the SiO2@Pd-PAMAM core-shell microspheres catalyzed the hydrogenation of phenylacetylene to ethylbenzene. The hydrogenation of phenylacetylene was found to be slightly slower than that of styrene (Table 3, entry 4). This was, however, to be expected considering the fact that the hydrogenation of phenylacetylene to ethylbenzene goes through two hydrogenation steps, i.e., phenylacetylene to styrene and then styrene to ethylbenzene. The catalyst, nevertheless, still exhibited high catalytic activity and TOF even for such two-step hydrogenation reaction. The hydrogenation of another reactant, cyclohexene, took place with almost ˜100% conversion in 20 minutes in the presence of the SiO2@Pd-PAMAM core-shell microspheres under the same reaction condition (Table 3, entry 5). In addition, the SiO2@Pd-PAMAM core-shell microspheres catalyzed n-hexene with ˜100% conversion in 60 minutes (Table 3, entry 6). More interestingly, although ketones undergo hydrogenation rather relatively slowly (Deshmukh et al. (2008) Catal. Lett., 120:257-260), the SiO2@Pd-PAMAM core-shell microspheres catalyzed the hydrogenation of acetone and acetylacetone efficiently and with high TOF. The catalytic hydrogenation of acetone with SiO2@Pd-PAMAM core-shell microspheres gave a sole product, isopropanol, with ˜100% conversion in 2 hours at 50° C., whereas the catalytic hydrogenation acetylacetonate gave 4-hydroxypentan-2-one with 95% conversion in 2 hours (Table 3, entries 7 and 8).

後処理

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出典と根拠

ORDレコード
ord-5d8d880ac3314ce881507fa5db2fb781
出典データセット
uspto-grants-2016_03
特許番号
US09283545B2

反応ノート

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