(E)-9-(3-Isopropyl-2-methoxy-phenyl)-6-methyl-3-oxo-non-6-enoic acid (1S,2S,5R)-5-methyl-2-[1-methyl-1-(4-nitro-phenyl)-ethyl]-cyclohexyl ester

Base Information

Chemical Name:(E)-9-(3-Isopropyl-2-methoxy-phenyl)-6-methyl-3-oxo-non-6-enoic acid (1S,2S,5R)-5-methyl-2-[1-methyl-1-(4-nitro-phenyl)-ethyl]-cyclohexyl ester
CAS No.:322640-53-9
Molecular Formula:C₃₆H₄₉NO₆
Molecular Weight:591.788
Hs Code.:

Synonyms:(E)-9-(3-Isopropyl-2-methoxy-phenyl)-6-methyl-3-oxo-non-6-enoic acid (1S,2S,5R)-5-methyl-2-[1-methyl-1-(4-nitro-phenyl)-ethyl]-cyclohexyl ester

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Chemical Property of (E)-9-(3-Isopropyl-2-methoxy-phenyl)-6-methyl-3-oxo-non-6-enoic acid (1S,2S,5R)-5-methyl-2-[1-methyl-1-(4-nitro-phenyl)-ethyl]-cyclohexyl ester

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Technology Process of (E)-9-(3-Isopropyl-2-methoxy-phenyl)-6-methyl-3-oxo-non-6-enoic acid (1S,2S,5R)-5-methyl-2-[1-methyl-1-(4-nitro-phenyl)-ethyl]-cyclohexyl ester

There total 9 articles about (E)-9-(3-Isopropyl-2-methoxy-phenyl)-6-methyl-3-oxo-non-6-enoic acid (1S,2S,5R)-5-methyl-2-[1-methyl-1-(4-nitro-phenyl)-ethyl]-cyclohexyl ester 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:

: 89-82-7,90449-51-7
pulegone

: 322640-53-9
(E)-9-(3-Isopropyl-2-methoxy-phenyl)-6-methyl-3-oxo-non-6-enoic acid (1S,2S,5R)-5-methyl-2-[1-methyl-1-(4-nitro-phenyl)-ethyl]-cyclohexyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: CuI / tetrahydrofuran

2: LiAlH₄ / tetrahydrofuran / 12 h / 20 °C

3: 92 percent / 4-(dimethylamino)-pyridine / pyridine / 22 h / 20 °C

4: 95 percent / ammonium nitrate; trifluoroacetic anhydride / CHCl₃ / 5 h / 20 °C

5: 92 percent / KOH / methanol; H₂O / 3 h / Heating

6: 4-(dimethylamino)pyridine / toluene / Heating

With dmap; potassium hydroxide; copper(l) iodide; lithium aluminium tetrahydride; ammonium nitrate; trifluoroacetic anhydride; In tetrahydrofuran; pyridine; methanol; chloroform; water; toluene; 1: Grignard reaction;
DOI:10.1021/ol0068243

Reference yield:

: 322640-04-0
(1S,2S,5R)-5-methyl-2-[1-methyl-(4-nitrophenyl)ethyl]cyclohexyl acetate

: 322640-53-9
(E)-9-(3-Isopropyl-2-methoxy-phenyl)-6-methyl-3-oxo-non-6-enoic acid (1S,2S,5R)-5-methyl-2-[1-methyl-1-(4-nitro-phenyl)-ethyl]-cyclohexyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / KOH / methanol; H₂O / 3 h / Heating

2: 4-(dimethylamino)pyridine / toluene / Heating

With dmap; potassium hydroxide; In methanol; water; toluene;
DOI:10.1021/ol0068243

Reference yield:

: 322640-03-9
(1S,2S,5R)-5-methyl-2-[1-methyl-(1-phenyl)ethyl]cyclohexyl acetate

: 322640-53-9
(E)-9-(3-Isopropyl-2-methoxy-phenyl)-6-methyl-3-oxo-non-6-enoic acid (1S,2S,5R)-5-methyl-2-[1-methyl-1-(4-nitro-phenyl)-ethyl]-cyclohexyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / ammonium nitrate; trifluoroacetic anhydride / CHCl₃ / 5 h / 20 °C

2: 92 percent / KOH / methanol; H₂O / 3 h / Heating

3: 4-(dimethylamino)pyridine / toluene / Heating

With dmap; potassium hydroxide; ammonium nitrate; trifluoroacetic anhydride; In methanol; chloroform; water; toluene;
DOI:10.1021/ol0068243