Propanoic acid, 2,2-dimethyl-, 4-[[4-[2-(hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3,4-dihydro-4- hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran-7-yl ester

Base Information

Chemical Name:Propanoic acid, 2,2-dimethyl-, 4-[[4-[2-(hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3,4-dihydro-4- hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran-7-yl ester
CAS No.:738601-50-8
Molecular Formula:C36H45NO6
Molecular Weight:587.756
Hs Code.:

Propanoic acid, 2,2-dimethyl-,
4-[[4-[2-(hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3,4-dihydro-4-
hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran-7-yl ester

Synonyms:

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Chemical Property of Propanoic acid, 2,2-dimethyl-, 4-[[4-[2-(hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3,4-dihydro-4- hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran-7-yl ester

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Technology Process of Propanoic acid, 2,2-dimethyl-, 4-[[4-[2-(hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3,4-dihydro-4- hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran-7-yl ester

There total 5 articles about Propanoic acid, 2,2-dimethyl-, 4-[[4-[2-(hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3,4-dihydro-4- hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran-7-yl 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:

: 444643-83-8
2,2-dimethyl-propanoic acid 3-(4-methoxyphenyl)-4-oxo-4H-1-benzopyran-7-yl ester

: 738601-50-8
2,2-dimethyl-propanoic acid 4-[[4-[2-(hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3,4-dihydro-4-hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran-7-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: H₂ / Pd/C / acetone; H₂O / 20 °C / 1551.44 Torr

2.1: Mg / tetrahydrofuran / Heating

2.2: 50 percent / tetrahydrofuran / -20 - 20 °C

3.1: H₂ / Pd/C / ethyl acetate; H₂O / 20 °C / 2585.74 Torr

4.1: K₂CO₃ / acetone / Heating

With hydrogen; potassium carbonate; magnesium; palladium on activated charcoal; In tetrahydrofuran; water; ethyl acetate; acetone; 2.2: Grignard addition;
DOI:10.1016/j.bmc.2004.05.015

Reference yield:

: 444643-85-0
2,2-dimethyl-propanoic acid 3,4-dihydro-4-hydroxy-3-(4-methoxyphenyl)-4-[[4-(phenylmethoxy)phenyl]-methyl]-2H-1-benzopyran-7-yl ester

: 738601-50-8
2,2-dimethyl-propanoic acid 4-[[4-[2-(hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3,4-dihydro-4-hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran-7-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd/C / ethyl acetate; H₂O / 20 °C / 2585.74 Torr

2: K₂CO₃ / acetone / Heating

With hydrogen; potassium carbonate; palladium on activated charcoal; In water; ethyl acetate; acetone;
DOI:10.1016/j.bmc.2004.05.015

Reference yield:

: 485-72-3
7-Hydroxy-3-(4-methoxy-phenyl)-chromen-4-on

: 738601-50-8
2,2-dimethyl-propanoic acid 4-[[4-[2-(hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3,4-dihydro-4-hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran-7-yl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: K₂CO₃ / acetonitrile / 20 °C

2.1: H₂ / Pd/C / acetone; H₂O / 20 °C / 1551.44 Torr

3.1: Mg / tetrahydrofuran / Heating

3.2: 50 percent / tetrahydrofuran / -20 - 20 °C

4.1: H₂ / Pd/C / ethyl acetate; H₂O / 20 °C / 2585.74 Torr

5.1: K₂CO₃ / acetone / Heating

With hydrogen; potassium carbonate; magnesium; palladium on activated charcoal; In tetrahydrofuran; water; ethyl acetate; acetone; acetonitrile; 3.2: Grignard addition;
DOI:10.1016/j.bmc.2004.05.015