ethyl {4-cyano-4-[3-(2,3-dihydro-1H-inden-2-yloxy)-4-methoxyphenyl]piperidin-1-yl}acetate

Base Information

Chemical Name:ethyl {4-cyano-4-[3-(2,3-dihydro-1H-inden-2-yloxy)-4-methoxyphenyl]piperidin-1-yl}acetate
CAS No.:401519-05-9
Molecular Formula:C₂₆H₃₀N₂O₄
Molecular Weight:434.535
Hs Code.:

Synonyms:ethyl {4-cyano-4-[3-(2,3-dihydro-1H-inden-2-yloxy)-4-methoxyphenyl]piperidin-1-yl}acetate

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Chemical Property of ethyl {4-cyano-4-[3-(2,3-dihydro-1H-inden-2-yloxy)-4-methoxyphenyl]piperidin-1-yl}acetate

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Technology Process of ethyl {4-cyano-4-[3-(2,3-dihydro-1H-inden-2-yloxy)-4-methoxyphenyl]piperidin-1-yl}acetate

There total 6 articles about ethyl {4-cyano-4-[3-(2,3-dihydro-1H-inden-2-yloxy)-4-methoxyphenyl]piperidin-1-yl}acetate 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: 77.0%

: 4254-29-9
indan-2-ol

: 401519-03-7
ethyl [4-cyano-4-(3-hydroxy-4-methoxyphenyl)piperidin-1-yl]acetate

: 401519-05-9
ethyl {4-cyano-4-[3-(2,3-dihydro-1H-inden-2-yloxy)-4-methoxyphenyl]piperidin-1-yl}acetate

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 20 ℃; for 15h;
DOI:10.1016/j.bmc.2004.06.032

Reference yield:

: 1699-39-4
2-(3-(benzyloxy)-4-methoxyphenyl)acetonitrile

: 401519-05-9
ethyl {4-cyano-4-[3-(2,3-dihydro-1H-inden-2-yloxy)-4-methoxyphenyl]piperidin-1-yl}acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: LiHMDS / tetrahydrofuran / 1 h / -78 °C

1.2: 93 percent / tetrahydrofuran / 1.5 h / -78 °C

2.1: ozone / CH₂Cl₂ / 0.42 h / -78 °C

2.2: Ph₃P / CH₂Cl₂ / 1.5 h / -78 - 20 °C

3.1: NaBH(OAc)3; AcOH / 1,2-dichloro-ethane / 3 h / 20 °C

4.1: 92 percent / H₂ / Pd/C / ethanol / 2.5 h / atmospheric pressure

5.1: 77 percent / PPh₃; diethyl azodicarboxylate / tetrahydrofuran / 15 h / 20 °C

With hydrogen; sodium tris(acetoxy)borohydride; ozone; acetic acid; triphenylphosphine; lithium hexamethyldisilazane; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1016/j.bmc.2004.06.032

Reference yield:

: 763109-95-1
1-(3-benzyloxy-4-methoxyphenyl)cyclopen-3-ene-1-carbonitrile

: 401519-05-9
ethyl {4-cyano-4-[3-(2,3-dihydro-1H-inden-2-yloxy)-4-methoxyphenyl]piperidin-1-yl}acetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: ozone / CH₂Cl₂ / 0.42 h / -78 °C

1.2: Ph₃P / CH₂Cl₂ / 1.5 h / -78 - 20 °C

2.1: NaBH(OAc)3; AcOH / 1,2-dichloro-ethane / 3 h / 20 °C

3.1: 92 percent / H₂ / Pd/C / ethanol / 2.5 h / atmospheric pressure

4.1: 77 percent / PPh₃; diethyl azodicarboxylate / tetrahydrofuran / 15 h / 20 °C

With hydrogen; sodium tris(acetoxy)borohydride; ozone; acetic acid; triphenylphosphine; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1016/j.bmc.2004.06.032