(2R,6R)-4-(2-Benzyloxy-ethyl)-2,6-diphenyl-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl ester

Base Information

• Chemical Name: (2R,6R)-4-(2-Benzyloxy-ethyl)-2,6-diphenyl-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl ester
• CAS No.: 127941-21-3
• Molecular Formula: C₂₈H₂₉NO₃
• Molecular Weight: 427.543
• Mol file: 127941-21-3.mol

Synonyms:(2R,6R)-4-(2-Benzyloxy-ethyl)-2,6-diphenyl-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl ester

Chemical Property of (2R,6R)-4-(2-Benzyloxy-ethyl)-2,6-diphenyl-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R,6R)-4-(2-Benzyloxy-ethyl)-2,6-diphenyl-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl ester

There total 5 articles about (2R,6R)-4-(2-Benzyloxy-ethyl)-2,6-diphenyl-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl 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: 95.0%

C19H20O (127941-20-2) + methyl N-phenylmethylenecarbamate (27593-61-9) → C28H29NO3 + (2R,6R)-4-(2-Benzyloxy-ethyl)-2,6-diphenyl-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl ester (127941-21-3)

Guidance literature:

With boron trifluoride diethyl etherate; In toluene; at -30 - 20 ℃; for 0.75h; optical yield given as %de; Inert atmosphere;

DOI:10.1021/ol100426m

Reference yield: 95.0%

benzylidene-carbamic acid methyl ester (27593-61-9) + C19H20O (127941-20-2) → (2R,6R)-4-(2-Benzyloxy-ethyl)-2,6-diphenyl-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl ester (127941-21-3)

Guidance literature:

boron trifluoride diethyl etherate; In toluene; at -30 - 23 ℃; for 0.5h;

DOI:10.1016/S0040-4039(01)93481-1

Reference yield:

Benzyloxymethyl chloride (3587-60-8) → (2R,6R)-4-(2-Benzyloxy-ethyl)-2,6-diphenyl-3,6-dihydro-2H-pyridine-1-carboxylic acid methyl ester (127941-21-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 75 percent / zinc bromide / CH₂Cl₂ / 1 h / 23 °C

2: 77 percent / tetrahydrofuran / 1.) -78 deg C, 30 min, 2.) 0 deg C, 30 min

3: 95 percent / boron trifluoride etherate / toluene / 0.5 h / -30 - 23 °C

boron trifluoride diethyl etherate; zinc dibromide; In tetrahydrofuran; dichloromethane; toluene;

DOI:10.1016/S0040-4039(01)93481-1

upstream raw materials:

benzylidene-carbamic acid methyl ester

C₁₉H₂₀O

Benzyloxymethyl chloride

{(1E)-3-[(trimethylsilyl)oxy]buta-1,3-dien-1-yl}benzene

Downstream raw materials:

2,6-Diphenyl-1-aza-bicyclo[2.2.2]octane

trans-2,6-diphenylquinuclidine

2-((2S,6S)-2,6-Diphenyl-piperidin-4-yl)-ethanol

(2R,6R)-4-(2-Hydroxy-ethyl)-2,6-diphenyl-piperidine-1-carboxylic acid methyl ester