(2R)-2-<(3,4-Dimethoxybenzoyl)methyl>-N-<(4-methoxyphenyl)acetyl>piperidine

Base Information

Chemical Name:(2R)-2-<(3,4-Dimethoxybenzoyl)methyl>-N-<(4-methoxyphenyl)acetyl>piperidine
CAS No.:167933-98-4
Molecular Formula:C₂₄H₂₉NO₅
Molecular Weight:411.498
Hs Code.:

Synonyms:(2R)-2-<(3,4-Dimethoxybenzoyl)methyl>-N-<(4-methoxyphenyl)acetyl>piperidine

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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 (2R)-2-<(3,4-Dimethoxybenzoyl)methyl>-N-<(4-methoxyphenyl)acetyl>piperidine

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Technology Process of (2R)-2-<(3,4-Dimethoxybenzoyl)methyl>-N-<(4-methoxyphenyl)acetyl>piperidine

There total 12 articles about (2R)-2-<(3,4-Dimethoxybenzoyl)methyl>-N-<(4-methoxyphenyl)acetyl>piperidine 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: 79.0%

: (2R)-2-<(2RS)-2-(3,4-Dimethoxyphenyl)-2-hydroxyethyl>-N-<(4-methoxyphenyl)acetyl>piperidine

: 167933-98-4
(2R)-2-<(3,4-Dimethoxybenzoyl)methyl>-N-<(4-methoxyphenyl)acetyl>piperidine

Guidance literature:: With dipyridinium dichromate; 4 A molecular sieve; In dichloromethane; for 5h; Ambient temperature;
DOI:10.1021/jo00124a025

Reference yield:

: C₁₅H₂₁NO₃

: 4693-91-8
4-methoxyphenyl-acetic chloride

: 167933-98-4
(2R)-2-<(3,4-Dimethoxybenzoyl)methyl>-N-<(4-methoxyphenyl)acetyl>piperidine

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 12h;
DOI:10.1055/s-0031-1290457

Reference yield:

: (6RS)-N-<(2S)-2-<(Benzyloxy)methyl>pyrrolidino>-6-methoxy-2-piperidinone

: 167933-98-4
(2R)-2-<(3,4-Dimethoxybenzoyl)methyl>-N-<(4-methoxyphenyl)acetyl>piperidine

Guidance literature:: Multi-step reaction with 4 steps

1: BF₃*Et₂O / CH₂Cl₂ / 1 h / Ambient temperature

2: 64 percent / BF₃*THF / tetrahydrofuran / 1.) room temp., 15 min, 2.) reflux, 24 h

3: 85 percent / 5percent aq. NaOH / CH₂Cl₂ / 0.67 h

4: 79 percent / PDC, 4 Angstroem molecular sieves / CH₂Cl₂ / 5 h / Ambient temperature

With sodium hydroxide; dipyridinium dichromate; boron trifluoride-tetrahydrofuran complex; 4 A molecular sieve; boron trifluoride diethyl etherate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo00124a025