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ChemicalBook CAS DataBase List Indoline

Indoline synthesis

13synthesis methods
-

Yield:496-15-1 99%

Reaction Conditions:

with hydrogen in water at 100; under 22502.3 Torr; for 10 h;

Steps:

3.2. Hydrogenation reaction in aqueous phase

General procedure: To showcase the applicability of this novel catalyst, the hydrogenationwas utilized for the other N-heterocyclic compounds. Asshown in Table 4, the hydrogenation of pyridine and 4-methylpyridinecould afford the desired product in excellent yield without by-products(Table 4, entries 1 and 2) although the reactivity of 4-methylpyridinewas somewhat less than that of pyridine, and a slightly longer reactiontime (7.5 h) was needed for full conversion (Table 4, entry 2). Additionally,indole was entirely transformed to dihydroindole and quinolinewas completely converted to 1,2,3,4-tetrahydroquinoline withhigh selectivity, respectively (Table 4, entries 3 and 4).

References:

Qian, Wei;Lin, Lina;Qiao, Yunxiang;Zhao;Xu, Zichen;Gong, Honghui;Li;Chen;Huang, Rong;Hou, Zhenshan [Applied Catalysis A: General,2019,vol. 585,art. no. 117183]

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