6-methoxy-1-(1-trityl-1H-imidazol-4-ylmethyl)-3,4-dihydro-1H-naphthalen-2-one

Base Information

Chemical Name:6-methoxy-1-(1-trityl-1H-imidazol-4-ylmethyl)-3,4-dihydro-1H-naphthalen-2-one
CAS No.:620171-87-1
Molecular Formula:C₃₄H₃₀N₂O₂
Molecular Weight:498.624
Hs Code.:

6-methoxy-1-(1-trityl-1<i>H</i>-imidazol-4-ylmethyl)-3,4-dihydro-1<i>H</i>-naphthalen-2-one

Synonyms:6-methoxy-1-(1-trityl-1H-imidazol-4-ylmethyl)-3,4-dihydro-1H-naphthalen-2-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 6-methoxy-1-(1-trityl-1H-imidazol-4-ylmethyl)-3,4-dihydro-1H-naphthalen-2-one

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Technology Process of 6-methoxy-1-(1-trityl-1H-imidazol-4-ylmethyl)-3,4-dihydro-1H-naphthalen-2-one

There total 2 articles about 6-methoxy-1-(1-trityl-1H-imidazol-4-ylmethyl)-3,4-dihydro-1H-naphthalen-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 66.0%

: 620171-81-5
6-methoxy-1-(1-trityl-1H-imidazol-4-ylmethylene)-3,4-dihydro-1H-naphthalen-2-one

: 620171-87-1
6-methoxy-1-(1-trityl-1H-imidazol-4-ylmethyl)-3,4-dihydro-1H-naphthalen-2-one

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; for 144h;
DOI:10.1081/SCC-120021500

Reference yield:

: 2472-22-2
6-methoxy-2-tetralone

: 620171-87-1
6-methoxy-1-(1-trityl-1H-imidazol-4-ylmethyl)-3,4-dihydro-1H-naphthalen-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 66 percent / piperidine / benzene / 22 h / Heating

2: 66 percent / H₂ / 10 percent Pd/C / ethyl acetate / 144 h

With piperidine; hydrogen; palladium on activated charcoal; In ethyl acetate; benzene;
DOI:10.1081/SCC-120021500